WO2015106215A2 - Pharmaceutical compositions comprising 15-hepe and methods of treating asthma and lung disorders using same - Google Patents

Pharmaceutical compositions comprising 15-hepe and methods of treating asthma and lung disorders using same Download PDF

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Publication number
WO2015106215A2
WO2015106215A2 PCT/US2015/011054 US2015011054W WO2015106215A2 WO 2015106215 A2 WO2015106215 A2 WO 2015106215A2 US 2015011054 W US2015011054 W US 2015011054W WO 2015106215 A2 WO2015106215 A2 WO 2015106215A2
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WO
WIPO (PCT)
Prior art keywords
day
per day
hepe
per
pharmaceutical composition
Prior art date
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PCT/US2015/011054
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French (fr)
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WO2015106215A3 (en
Inventor
Mehar Manku
John Climax
Kevin Duffy
Original Assignee
Mehar Manku
John Climax
Kevin Duffy
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Publication date
Priority to KR1020167021684A priority Critical patent/KR20160132372A/en
Priority to JP2016563894A priority patent/JP2017505809A/en
Priority to MX2016008953A priority patent/MX2016008953A/en
Priority to AU2015204531A priority patent/AU2015204531B2/en
Application filed by Mehar Manku, John Climax, Kevin Duffy filed Critical Mehar Manku
Priority to CN201580008336.5A priority patent/CN106029051A/en
Priority to BR112016015997A priority patent/BR112016015997A2/en
Priority to EP15735225.3A priority patent/EP3091959A4/en
Priority to RU2016132762A priority patent/RU2685706C2/en
Priority to SG11201605601UA priority patent/SG11201605601UA/en
Priority to CA2935986A priority patent/CA2935986A1/en
Publication of WO2015106215A2 publication Critical patent/WO2015106215A2/en
Publication of WO2015106215A3 publication Critical patent/WO2015106215A3/en
Priority to IL246623A priority patent/IL246623A0/en
Priority to PH12016501371A priority patent/PH12016501371A1/en
Priority to ZA2016/05492A priority patent/ZA201605492B/en

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Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/327Peroxy compounds, e.g. hydroperoxides, peroxides, peroxyacids
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/185Acids; Anhydrides, halides or salts thereof, e.g. sulfur acids, imidic, hydrazonic or hydroximic acids
    • A61K31/19Carboxylic acids, e.g. valproic acid
    • A61K31/20Carboxylic acids, e.g. valproic acid having a carboxyl group bound to a chain of seven or more carbon atoms, e.g. stearic, palmitic, arachidic acids
    • A61K31/202Carboxylic acids, e.g. valproic acid having a carboxyl group bound to a chain of seven or more carbon atoms, e.g. stearic, palmitic, arachidic acids having three or more double bonds, e.g. linolenic
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K45/00Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
    • A61K45/06Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00Drugs for disorders of the respiratory system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00Drugs for disorders of the respiratory system
    • A61P11/06Antiasthmatics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00Drugs for disorders of the respiratory system
    • A61P11/08Bronchodilators
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00Drugs for disorders of the respiratory system
    • A61P11/10Expectorants
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P5/00Drugs for disorders of the endocrine system
    • A61P5/38Drugs for disorders of the endocrine system of the suprarenal hormones
    • A61P5/40Mineralocorticosteroids, e.g. aldosterone; Drugs increasing or potentiating the activity of mineralocorticosteroids
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K2300/00Mixtures or combinations of active ingredients, wherein at least one active ingredient is fully defined in groups A61K31/00 - A61K41/00

Definitions

  • compositions comprising 15-HEPE used singly or in combination with other active agents for the treatment and/or prevention of asthma and lung disorders.
  • Asthma is a chronic lung disease that inflames and narrows the airways.
  • the narrowing of the airways is a result of muscle tightening as well as inflammation.
  • the narrowing results in less air flowing into the lungs.
  • Asthmatics tend to react strongly to airborne substances, leading to increases in mucus production; staring a chain reaction toward a full blown asthmatic attack. Symptoms include recurring periods of wheezing, chest tightness, shortness of breath, coughing and in extreme cases, can be fatal.
  • the predominant risk factors associated with childhood-onset asthma are genetic predisposition, a family history of allergy and asthma, viral respiratory infections, bacterial colonization, allergic sensitization and tobacco exposure.
  • Viral infections are another risk factor for developing early childhood asthma.
  • Long-term follow-up studies have shown that whez episodes associated with rhinovirus infection are a strong predictor of asthma by the age of 6 years.
  • studies have also reported that children with early whez symptoms and a predisposition to asthma and atopy are at increased risk of lower respiratory infection. Therefore, the direction of causality of viral infection and the development of asthma is still unclear.
  • asthma can be a comorbid condition of other diseases. Asthma is a common comorbid factor in sickle cell disease (SCD). However, the incidence of asthma in SCD is much higher than expected compared to rates in the general population. Whether "asthma" in SCD is purely related to genetic and environmental factors or rather is the consequence of the underlying hemolytic and inflammatory state is a topic of recent debate. Regardless of the etiology, hypoxemia induced by bronchoconstriction and inflammation associated with asthma exacerbations will contribute to a cycle of sickling and subsequent complications of SCD. Recent studies confirm that asthma predisposes to complications of SCD such as pain crises, acute chest syndrome, and stroke, and is associated with increased mortality.
  • SCD sickle cell disease
  • COPD chronic obstructive pulmonary disease
  • COPD encompasses both chronic bronchitis and emphysema and is characterized by airway narrowing, air trapping, alveolar destruction, and excessive airway inflammation and oxidative stress.
  • Cigarette smoke (CS) is the most common cause of COPD. In COPD there are marked increases in both inflammation and oxidative stress, which can be replicated in mice by exposing them to tobacco smoke.
  • compositions comprising fatty acid agents including, for example, 15-HEPE (also referred to as “15-OHEPA”) used singly, in combination and/or in combination with a second active agent for treatment of lung diseases or disorders, such as asthma or COPD.
  • 15-HEPE also referred to as “15-OHEPA”
  • a second active agent for treatment of lung diseases or disorders such as asthma or COPD.
  • the present disclosure also provides methods for treating a lung disease or disorder mediated by 15-HEPE in a subject in need thereof comprising administering to subject a pharmaceutical composition comprising a therapeutically effective amount of 15- HEPE or combinations thereof.
  • the pharmaceutical composition comprises about 5 g to about 10,000 mg of 15-HEPE, for example about 50 g to about 4,000 mg of 15-HEPE.
  • the method comprises orally administering about 50 mg to about 4,000 mg of 15-HEPE to the subject per day.
  • the present disclosure also provides methods for treating a lung disease or disorder mediated by 15-HEPE in a subject in need thereof comprising administering to a subject a pharmaceutical composition comprising a therapeutically effective amount of 15- HEPE.
  • the pharmaceutical composition comprises about 5 g to about 10,000 mg of 15-HEPE, for example about 50 pg to about 4,000 mg of 15-HEPE.
  • the method comprises administering about 50 mg to about 4,000 mg of 15-HEPE to the subject per day.
  • the pharmaceutical composition comprises one or more pharmaceutically acceptable excipients.
  • the pharmaceutical composition comprises a second active agent.
  • the second active agent is one or more of: short- acting bronchodilators (i.e. short-acting beta agonists), long-acting bronchodilators (i.e. long-acting beta agonists), phosphodiesterase-4 ("PDE4") inhibitors, corticosteroids, leukotriene receptor antagonists, expectorants and methylxanthines.
  • the step of administering comprises delivering the pharmaceutical composition to a lung of the subject by dry-powder inhaler.
  • the pharmaceutical composition is in dry powder form.
  • the step of administering comprises delivering the pharmaceutical composition to a lung of the subject by metered dose inhaler.
  • the pharmaceutical composition is in powder form.
  • the pharmaceutical composition further comprises a propellant.
  • the step of administering comprises delivering the pharmaceutical composition to a lung of the subject by nebulizer.
  • the pharmaceutical composition is a solution comprising a solvent system.
  • the solvent system comprises an alcohol and/or a polyol.
  • the solvent system does not include an alcohol or a polyol.
  • the pharmaceutical composition is a suspension.
  • compositions of the invention are in the form of solid dosage forms.
  • suitable solid dosage forms include tablets (e.g. suspension tablets, bite suspension tablets, rapid dispersion tablets, chewable tablets, melt tablets, effervescent tablets, bilayer tablets, etc), caplets, capsules (e.g. a soft or a hard gelatin capsule filled with solid and/or liquids), powder (e.g.
  • a packaged powder a dispensable powder or an effervescent powder
  • lozenges lozenges, sachets, cachets, troches, pellets, granules, microgranules, encapsulated microgranules, powder aerosol formulations, or any other solid dosage form reasonably adapted for oral administration.
  • the pharmaceutical composition is formulated for intravenous or intramuscular injection by methods known in the art.
  • the method comprises co-administering a pharmaceutical composition comprising 15-HEPE with a second active agent.
  • the second active agent is co-formulated with the pharmaceutical composition.
  • the second active agent is administered simultaneously, concomitantly, or within 1 to 24 hours of the pharmaceutical composition comprising 15-HEPE.
  • the 15-HEPE is in the form of an ester.
  • the compositions comprise a Ci - C 5 alkyl ester of 15-HEPE.
  • the compositions comprise a methyl ester, propyl ester, or butyl ester.
  • the 15-HEPE is in the form of a pharmaceutically acceptable salt.
  • the 15-HEPE comprises lithium, mono, di- or triglyceride or any other ester or 15-HEPE.
  • the 15-HEPE comprises salts, including but not limited to sodium, lysine, ornithine, piperazine or meglumine.
  • the 15-HEPE the free acid form of 15-HEPE.
  • 15-HEPE present in a composition of the invention comprises at least 90% by weight 15-HEPE (as the term "15-HEPE" is defined and exemplified herein).
  • 15-HEPE compositions can comprise even higher purity compositions, for example at least 95% by weight 15-HEPE or at least 97% by weight 15- HEPE, wherein the 15-HEPE is any form of 15-HEPE as set forth herein.
  • 15-HEPE is present in a composition of the invention in an amount of about 5 g to about 10,000 mg, about 25 mg to about 7500mg, 50 mg to about 5000 mg, about 75 mg to about 2500 mg, about 100 mg to about 1000 mg, or about 50 ig to about 1000 g, for example about 5 g, about 10 g, about 15 g, about 20 g, about 25 [ig, about 30 g, about 35 g, about 40 g, about 45 g, about 50 g, about 55 about 60 g, about 65 [ig, about 70 [ig, about 75 [ig, about 80 [ig, about 85 [ig, about 90 [ig, about 95 [ig, about 100 [ig, about 105 [ig, about 1 10 [ig, about 1 15 [ig, about 120 [ig, about 125 [ig, about 130 [ig, about 135 [ig, about 140 [ig, about 145 [ig, about 150 [ig,
  • a composition of the invention contains not more than about 10%, not more than about 9%, not more than about 8%, not more than about 7%, not more than about 6%, not more than about 5%, not more than about 4%, not more than about 3%, not more than about 2%, not more than about 1 %, or not more than about 0.5%, by weight of other omega-3 fatty acids such eicosapentaenoic acid, alpha linolenic acid, docosahexaenoic acid, docosapentaenoic acid or derivatives thereof.
  • omega-3 fatty acids such eicosapentaenoic acid, alpha linolenic acid, docosahexaenoic acid, docosapentaenoic acid or derivatives thereof.
  • 15-HEPE represents at least about 60%, at least about 70%, at least about 80%, at least about 90%, at least about 95%, at least about 97%, at least about 98%, at least about 99%, or 100%, by weight, of all fatty acids present in a composition of the invention.
  • the present disclosure provides a method for treating a lung disease or disorder comprising administering a pharmaceutical composition comprising 15-HEPE to a subject in need thereof.
  • FIG. 1 shows ventilatory pressure (mm Hg) changes following exposition of nebulized histamine doses after seven consecutive days of gavage with vehicle.
  • FIG. 2 shows ventilatory pressure (mm Hg) changes following exposition of nebulized histamine doses after seven consecutive days of gavage with bambuterol at 0.27 mg/kg/day.
  • FIG. 3 shows ventilatory pressure (mm Hg) changes following exposition of nebulized histamine doses after seven consecutive days of gavage with 15-HEPE at 50 mg/kg/day.
  • FIG. 4 shows ventilatory pressure (mm Hg) changes following exposition of nebulized histamine doses after seven consecutive days of gavage with 15-HEPE at 500 mg/kg/day.
  • FIG. 5 shows ventilatory pressure (mm Hg) changes following exposition of nebulized histamine doses after seven consecutive days of gavage with vehicle, bambuterol (0.27mg/kg/day),OH-EPA (50 mg/kg/day) and OH-EPA (500mg/kg/day).
  • lung disease refers to many disorders affecting the lungs, such as asthma, chronic obstructive pulmonary disease (“COPD”), infections like influenza, pneumonia and tuberculosis, lung cancer, and many other breathing problems.
  • COPD chronic obstructive pulmonary disease
  • compositions e.g., pharmaceutical compositions
  • formulations that comprise 15-HEPE. This agent has been found to improve lung ventilatory pressure in test animals when the animals were challenged with a bronchoconstrictor.
  • compositions comprising 15-HEPE in free acid or derivative form, used singly or in combination with additional active agents including, for example, short-acting bronchodilators (i.e. short-acting beta agonists), long- acting bronchodilators (i.e. long-acting beta agonists), phosphodiesterase-4 ("PDE4") inhibitors, corticosteroids, leukotriene receptor antagonists, expectorants and methylxanthines.
  • additional active agents including, for example, short-acting bronchodilators (i.e. short-acting beta agonists), long- acting bronchodilators (i.e. long-acting beta agonists), phosphodiesterase-4 ("PDE4") inhibitors, corticosteroids, leukotriene receptor antagonists, expectorants and methylxanthines.
  • additional active agents including, for example, short-acting bronchodilators (i.e. short-acting beta agonists), long- acting broncho
  • the compositions comprise about 50 g/mL to about 1 ,000 g/mL of 15-HEPE or derivative thereof.
  • Contemplated combinations include, without limitation, 15-HEPE and ipratropium, 15-HEPE and albuterol, 15-HEPE and levalbuterol, 15-HEPE with albuterol and levalbuterol, 15-HEPE and tiotropium, 15-HEPE and salmeterol, 15-HEPE and formoterol, 15-HEPE and aformoterol, 15-HEPE and prednisone, 15-HEPE and guaifenesin, 15-HEPE and aminophylline, 15-HEPE and theophylline, 15-HEPE and montelukast, 15-HEPE and zafirlukast, 15-HEPE and zileuton, 15-HEPE and pranlukast.
  • a composition comprising 15-HEPE includes a therapeutically effective
  • 15-Hydroxy-eicosa-5,8,1 1 ,13,17-pentaenoic acid (“15-HEPE”) is a derivative of EPA.
  • 15-HEPE refers to 15-HEPE in its free acid form (e.g, 15- hydroxy-eicosa-5,8,1 1 ,13,17-pentaenoic acid) and/or a pharmaceutically acceptable ester, derivative, conjugate or salt thereof, or mixtures of any of the foregoing.
  • the 15-HEPE is in the form of a Ci -4 alkyl ester such as methyl ester or ethyl ester form.
  • 15-HEPE derivative and “derivative of 15-HEPE” refer to compounds formed from the chemical conversion of 15-HEPE including, without limitation, esters, derivatives, conjugates or salts thereof, or mixtures of any of the foregoing.
  • esters, derivatives, conjugates or salts thereof or mixtures of any of the foregoing.
  • One of skill in the art will readily recognize from the chemical structure and other properties whether a given compound is a 15-HEPE derivative.
  • the invention provides pharmaceutical compositions, for example aerosolizable compositions, comprising of 15-HEPE.
  • the present disclosure provides pharmaceutical compositions comprising, for example, an amount (e.g., a therapeutically effective amount) of 15-HEPE.
  • the pharmaceutical composition comprises about 50 pg/mL to about 1 ,000 pg/mL of 15-HEPE, for example 50 pg/mL, 60 pg/mL, 70 pg/mL, 80 pg/mL, 90 pg/mL, 100 pg/mL, 1 10 pg/mL, 120 pg/mL, 130 pg/mL, 140 pg/mL, 150 pg/mL, 160 pg/mL, 170 pg/mL, 180 pg/mL, 190 pg/mL, 200 pg/mL, 210 pg/mL, 220 pg/mL, 230 pg/mL, 240 pg/mL, 250 pg/mL, 260
  • the pharmaceutical composition further comprises an additional active agent.
  • the pharmaceutical composition comprises an amount of the additional active agent that is less than the generally recognized therapeutically effective amount for that agent. In one embodiment, the pharmaceutical composition comprises an amount of the additional active agent that is equal to or greater than the generally recognized therapeutically effective amount for that agent.
  • the additional active agent has not previously been recognized as effective in the treatment of, including inhibition of, symptoms associated with lung diseases or disorders. In another embodiment, the additional active agent is approved for use in the treatment or prevention of a lung disease or disorder and/or the reduction of, including inhibition of, symptoms associated with a lung disease or disorder.
  • the additional active agent is a short-acting bronchodilator.
  • short-acting bronchodilator refers to the class of compounds that are generally recommended for treatment of intermittent symptoms associated with a lung disease or disorder.
  • short- acting bronchodilators include anticholinergics (e.g., ipratropium), beta-2-agonists (e.g., albuterol, levalbuterol), and combinations thereof (e.g., albuterol and ipratropium).
  • the method comprises administering the pharmaceutical composition comprising 15-HEPE and a short-acting bronchodilator in an amount sufficient to provide about 5 ig to about 2,000 [ig of short-acting bronchodilator to the subject per day, for example 5 [ig per day, 10 [ig per day, 18 [ig per day, 20 [ig per day, 25 [ig per day, 30 [ig per day, 35 [ig per day, 36 [ig per day, 40 [ig per day, 45 [ig per day, 50 [ig per day, 55 [ig per day, 60 [ig per day, 65 [ig per day, 70 [ig per day, 75 [ig per day, 80 [ig per day, 85 [ig per day, 90 [ig per day, 95 [ig per day, 100 [ig per day, 105 [ig per day, 1 10 g per day, 1 15 ig per day, 120 [ig per day, 125 [ig per day, 130
  • the additional active agent is a long-acting bronchodilator.
  • long-acting bronchodilator refers to the class of compounds that are generally recommended for treatment of persistent symptoms associated with a lung disease or disorder.
  • long-acting bronchodilators include anticholinergics (e.g., tiotropium), beta-2-agonists (e.g., salmeterol, formoterol, arformoterol), and combinations thereof.
  • the method comprises administering the pharmaceutical composition comprising 15-HEPE and a long-acting bronchodilator in an amount sufficient to provide about 5 g to about 100 g of long-acting bronchodilator to the subject per day, for example 5 g per day, 6 g per day, 7 g per day, 8 g per day, 9 g per day, 10 g per day, 1 1 g per day, 12 g per day, 13 g per day, 14 M9 per day, 15 M9 per day, 16 M9 per day, 17 M9 per day, 18 M9 per day, 19 M9 per day, 20 M9 per day, 21 M9 per day, 22 M9 per day, 23 M9 per day, 24 M9 per day, 25 M9 per day, 26 M9 per day, 27 M9 per day, 28 M9 per day, 29 M9 per day, 30 M9 per day, 31 M9 per day, 32 M9 per day, 33 M9 per day, 34 M9 per day, 35 M9 per day, 36 M9 per day,
  • the additional active agent is a phosphodiesterase-4 ("PDE4") inhibitor.
  • PDE4 phosphodiesterase-4
  • the terms "phosphodiesterase-4 inhibitor” and "PDE4" inhibitor each refer to the class of compounds that are generally recommended to help prevent exacerbations associated with COPD (e.g., roflumilast).
  • the method comprises administering the pharmaceutical composition comprising 15-HEPE and a PDE4 inhibitor in an amount sufficient to provide about 250 [ ⁇ g to about 1 ,000 [ ⁇ g of PDE4 inhibitor to the subject per day, for example 250 [ig per day, 275 [ig per day, 300 [ig per day, 325 [ig per day, 350 [ig per day, 375 [ig per day, 400 [ig per day, 425 [ig per day, 450 ig per day, 475 [ig per day, 500 [ig per day, 525 [ig per day, 550 [ig per day, 575 [ig per day, 600 [ig per day, 625 [ig per day, 650 [ig per day, 675 [ig per day, 700 [ig per day, 725 ig per day, 750 [ig per day, 775 [ig per day, 800 [ig per day, 825 [ig per day, 850 [ig per day, 875 [i
  • the additional active agent is a corticosteroid.
  • corticosteroid refers to the class of compounds that are generally recommended to treat asthma, COPD exacerbation, stable symptoms of COPD, or progressing symptoms of COPD.
  • corticosteroids include methylprednisolone, prednisolone, prednisone, beclomethasone, budesonide, flunisolide, fluticasone, mometasone, triamcinolone and combinations thereof.
  • the method comprises administering the pharmaceutical composition comprising 15-HEPE and a corticosteroid in an amount sufficient to provide about 50% to about 200% of the daily recommended corticosteroid dose to the subject per day, for example 50%, 55%, 60%, 65%, 70%, 75%, 80%, 85%, 90%, 95%, 100%, 105%, 1 10%, 1 15%, 120%, 125%, 130%, 135%, 140%, 145%, 150%, 155%, 160%, 165%, 170%, 175%, 180%, 185%, 190%, 195%, or 200% of the daily recommended corticosteroid dose per day.
  • the amount of a corticosteroid having a daily recommended dose of 40 mg per day to 80 mg per day could be present in a pharmaceutical formulation as disclosed herein (or administered according to a method disclosed herein) in an amount sufficient to provide from about 20 mg of the corticosteroid per day (i.e., 50% of the lowest recommended daily dose, 40 mg/day) to about 160 mg of the corticosteroid per day (i.e., 200% of the maximum daily recommended dose, 80 mg/day).
  • the corticosteroid is coformulated with the pharmaceutical composition comprising 15-HEPE.
  • the corticosteroid is in tablet or capsule form.
  • the method comprises separately co-administering a corticosteroid and a pharmaceutical composition comprising 15-HEPE.
  • the additional active agent is an expectorant.
  • the term “expectorant” refers to the class of compounds that are generally recommended to help prevent mucus from sticking to the airways of the lungs (e.g., guaifenesin).
  • the method comprises administering the pharmaceutical composition comprising 15-HEPE and an expectorant in an amount sufficient to provide about 100 mg to about 3,000 mg of expectorant to the subject per day, for example 100 mg per day, 200 mg per day, 300 mg per day, 400 mg per day, 500 mg per day, 600 mg per day, 700 mg per day, 800 mg per day, 900 mg per day, 1 ,000 mg per day, 1 ,100 mg per day, 1 ,200 mg per day, 1 ,300 mg per day, 1 ,400 mg per day, 1 ,500 mg per day, 1 ,600 mg per day, 1 ,700 mg per day, 1 ,800 mg per day, 1 ,900 mg per day, 2,000 mg per day, 2,100 mg per day, 2,200 mg per day, 2,300 mg per day, 2,400 mg per day, 2,500 mg per day, 2,600 mg per day, 2,700 mg per day, 2,800 mg per day, 2,900 mg per day, or 3,000 mg per day.
  • the method comprises separately coadminister
  • the additional active agent is a methylxanthine.
  • methylxanthine refers to the class of compounds that are generally recommended for relaxing the airways in the lungs, increasing the strength of the diaphragm, stimulating the breathing control centers in the brain, and/or remove mucus from the lungs.
  • methylxanthines include aminophylline, theophylline and combinations thereof.
  • the method comprises administering the pharmaceutical composition comprising 15-HEPE and a methylxanthine in an amount sufficient to provide about 100 mg to about 3,000 mg of methylxanthine to the subject per day, for example 100 mg per day, 200 mg per day, 300 mg per day, 400 mg per day, 500 mg per day, 600 mg per day, 700 mg per day, 800 mg per day, 900 mg per day, 1 ,000 mg per day, 1 ,100 mg per day, 1 ,200 mg per day, 1 ,300 mg per day, 1 ,400 mg per day, 1 ,500 mg per day, 1 ,600 mg per day, 1 ,700 mg per day, 1 ,800 mg per day, 1 ,900 mg per day, 2,000 mg per day, 2,100 mg per day, 2,200 mg per day, 2,300 mg per day, 2,400 mg per day, 2,500 mg per day, 2,600 mg per day, 2,700 mg per day, 2,800 mg per day, 2,900 mg per day, or 3,000 mg per day.
  • the method comprises separately co-administering an expectorant and a pharmaceutical composition comprising 15-HEPE.
  • the methylxanthine is administered separately as an intravenous solution.
  • a loading dose of the methylxanthine is also administered, with or without coadminstration of the 15- HEPE component.
  • any pharmaceutically acceptable excipient known to those of skill in the art may be used in pharmaceutical compositions according to the present disclosure.
  • Any excipient selected for use in the therapeutic compositions should be pharmaceutically acceptable and appropriate for the form in which the therapeutic composition will be used, e.g., aerosol, dry powder, capsule, tablet, cream, gel, milk, oil, lotion, and the like.
  • the excipient has an affinity for lung tissue, is well tolerated, and stable when used in an amount adequate to provide the desired consistency and ease of application.
  • a pharmaceutical composition according to the present disclosure may comprise one or more of: propellants, preservatives, amphiphilic agents, surfactants, coloring agents, flavorants, buffers, antioxidants, stabilizers, fragrances, emollients, emulsifiers, thickeners, texturizers, and the like.
  • the pharmaceutical composition comprises about 0.5 wt.% to about 5 wt.% of a surfactant, for example, about 0.5 wt.%, about 0.55 wt.%, about 0.6 wt.%, about 0.65 wt.%, about 0.7 wt.%, about 0.75 wt.%, about 0.8 wt.%, about 0.85 wt.%, about 0.9 wt.%, about 0.95 wt.%, about 1 wt.%, about 1 .05 wt.%, about 1 .1 wt.%, about 1 .15 wt.%, about 1 .2 wt.%, about 1 .25 wt.%, about 1 .3 wt.%, about 1 .35 wt.%, about 1 .4 wt.%, about 1 .45 wt.%, about 1 .5 wt.%, about 1 .55 wt.
  • a surfactant
  • the pharmaceutical composition comprises about 0.5 wt.% to about 5 wt.% of an emulsifier, for example, about 0.5 wt.%, about 0.55 wt.%, about 0.6 wt.%, about 0.65 wt.%, about 0.7 wt.%, about 0.75 wt.%, about 0.8 wt.%, about 0.85 wt.%, about 0.9 wt.%, about 0.95 wt.%, about 1 wt.%, about 1 .05 wt.%, about 1 .1 wt.%, about 1 .15 wt.%, about 1 .2 wt.%, about 1 .25 wt.%, about 1 .3 wt.%, about 1 .35 wt.%, about 1 .4 wt.%, about 1 .45 wt.%, about 1 .5 wt.%, about 1 .55 wt
  • the pharmaceutical composition comprises a stabilizer.
  • the pharmaceutical composition comprises about 0.1 wt.% to about 5 wt.% of a stabilizer, for example about 0.1 wt.%, about 0.1 1 wt.%, about 0.12 wt.%, about 0.13 wt.%, about 0.14 wt.%, about 0.15 wt.%, about 0.16 wt.%, about 0.17 wt.%, about 0.18 wt.%, about 0.19 wt.%, about 0.2 wt.%, about 0.21 wt.%, about 0.22 wt.%, about 0.23 wt.%, about 0.24 wt.%, about 0.25 wt.%, about 0.26 wt.%, about 0.27 wt.%, about 0.28 wt.%, about 0.29 wt.%, about 0.3 wt.%, about 0.31 wt.%, about 0.32 wt.
  • the pharmaceutical composition comprises one or more antioxidants.
  • the pharmaceutical composition comprises about 0.01 wt.% to about 2 wt.% of an antioxidant, for example about 0.01 wt.%, about 0.02 wt.%, about 0.03 wt.%, about 0.04 wt.%, about 0.05 wt.%, about 0.06 wt.%, about 0.07 wt.%, about 0.08 wt.%, about 0.09 wt.%, about 0.1 wt.%, about 0.1 1 wt.%, about 0.12 wt.%, about 0.13 wt.%, about 0.14 wt.%, about 0.15 wt.%, about 0.16 wt.%, about 0.17 wt.%, about 0.18 wt.%, about 0.19 wt.%, about 0.2 wt.%, about 0.21 wt.%, about 0.22 wt.%, about 0.23 wt.%
  • the pharmaceutical composition comprises a preservative.
  • the pharmaceutical composition comprises about 0.1 wt.% to about 5 wt.% of a preservative, for example about 0.1 wt.%, about 0.2 wt.%, about 0.3 wt.%, about 0.4 wt.%, about 0.5 wt.%, about 0.6 wt.%, about 0.7 wt.%, about 0.8 wt.%, about 0.9 wt.%, about 1 wt.%, about 1 .1 wt.%, about 1 .2 wt.%, about 1 .3 wt.%, about 1 .4 wt.%, about 1 .5 wt.%, about 1 .6 wt.%, about 1 .7 wt.%, about 1 .8 wt.%, about 1 .9 wt.%, about 2 wt.%, about 2.1 wt.%
  • the pharmaceutical composition comprises: about 50 g/mL to about 4,000 mg/mL of one or more of 15-HEPE and optionally a second active agent.
  • a composition for use in accordance with the disclosure can be formulated as one or more dosage units.
  • dose unit and “dosage unit” herein refer to a portion of a pharmaceutical composition that contains an amount of a therapeutic agent suitable for a single administration to provide a therapeutic effect.
  • dosage units may be administered one to a plurality (i.e. 1 to about 10, 1 to 8, 1 to 8, 1 to 4 or 1 to 2) of times per day, or as many times as needed to elicit a therapeutic response.
  • a composition including, for example, a pharmaceutical composition, as disclosed herein is formulated as an aerosol, a capsule, a tablet or other oral dosage form.
  • Such formulations may be stable and comprise an amount (e.g., a therapeutically effective amount) of 15-HEPE, in combination with one or more second active agents selected from the group consisting of: short-acting bronchodilators (i.e. short- acting beta agonists), long-acting bronchodilators (i.e. long-acting beta agonists), phosphodiesterase-4 ("PDE4") inhibitors, corticosteroids, leukotriene receptor antagonists, expectorants and methylxanthines.
  • PDE4 phosphodiesterase-4
  • compositions comprising 15-HEPE as disclosed herein may be determined by any method known in the art.
  • the pharmacodynamics of a composition comprising 15- HEPE as disclosed herein may be examined using a model of a lung disease or disorder.
  • the effects of a composition comprising a vehicle, a positive control or 15-HEPE on ventilator pressure in histamine challenged guinea pigs serves as a model for the pharmacodynamics in asthma.
  • guinea pigs are first dosed with compositions comprising a vehicle, a positive control or 15-HEPE for seven days.
  • the treated guinea pigs can then be anesthetized and exposed to a nebulized bronchoconstictor to determine if 15-HEPE can reduce the increase in ventilatory pressure induced by a bronchoconstrictor. This serves as an effective model for asthma and other lung diseases.
  • compositions and formulations disclosed herein may be used in the treatment of diseases and/or disorders including, for example, lung diseases and/or disorders such as asthma or COPD.
  • compositions of the invention are in the form of solid dosage forms for oral delivery.
  • suitable solid dosage forms include tablets (e.g. suspension tablets, bite suspension tablets, rapid dispersion tablets, chewable tablets, melt tablets, effervescent tablets, bilayer tablets, etc), caplets, capsules (e.g. a soft or a hard gelatin capsule filled with solid and/or liquids), powder (e.g.
  • a packaged powder a dispensable powder or an effervescent powder
  • lozenges lozenges, sachets, cachets, troches, pellets, granules, microgranules, encapsulated microgranules, powder aerosol formulations, or any other solid dosage form reasonably adapted for oral administration.
  • 15-HEPE is present in a composition of the invention in an amount of about 5 [ ⁇ g to about 10,000 mg, about 25 mg to about 7500mg, 50 mg to about 5000 mg, about 75 mg to about 2500 mg, about 100 mg to about 1000 mg, or about 50 ⁇ ig to about 1000 ⁇ ig, for example about 5 ⁇ ig, about 10 ⁇ ig, about 15 ⁇ ig, about 20 ⁇ ig, about 25 [ig, about 30 ⁇ ig, about 35 ⁇ ig, about 40 ⁇ ig, about 45 ⁇ ig, about 50 ⁇ ig, about 55 about 60 ⁇ ig, about 65 [ig, about 70 [ig, about 75 [ig, about 80 [ig, about 85 [ig, about 90 [ig, about 95 [ig, about 100 [ig, about 105 [ig, about 1 10 [ig, about 1 15 [ig, about 120 [ig, about 125 [ig, about 130 [ig, about 1
  • a composition of the invention contains not more than about 10%, not more than about 9%, not more than about 8%, not more than about 7%, not more than about 6%, not more than about 5%, not more than about 4%, not more than about 3%, not more than about 2%, not more than about 1%, or not more than about 0.5%, by weight of other omega-3 fatty acids such eicosapentaenoic acid, alpha linolenic acid, docosahexaenoic acid, docosapentaenoic acid or derivatives thereof.
  • omega-3 fatty acids such eicosapentaenoic acid, alpha linolenic acid, docosahexaenoic acid, docosapentaenoic acid or derivatives thereof.
  • 15-HEPE represents at least about 60%, at least about 70%, at least about 80%, at least about 90%, at least about 95%, at least about 97%, at least about 98%, at least about 99%, or 100%, by weight, of all fatty acids present in a composition of the invention.
  • the present disclosure provides a method for treating a disease or disorder mediated by 15-HEPE comprising administering a pharmaceutical composition comprising 15-HEPE to a subject in need thereof.
  • the pharmaceutical composition comprises about 50 g/mL to about 1,000 g/mL of 15-HEPE, for example about 50 pg/mL, about 60 pg/mL, about 70 pg/mL, about 80 pg/mL, about 90 g/mL, about 100 g/mL, about 110 g/mL, about 120 g/mL, about 130 g/mL, about 140 g/mL, about 150 g/mL, about 160 g/mL, about 170 g/mL, about 180 g/mL, about 190 g/mL, about 200 g/mL, about 210 g/mL, about 220 g/mL, about 230 g/mL, about 240 g/mL, about
  • the subject is administered about 5 Mg to about 4,000 mg of 15-HEPE per day, for example about 5 Mg/day to about 10,000 mg, about 25 mg to about 7500mg, 50 mg to about 5000 mg, about 75 mg to about 2500 mg, about 100 mg to about 1000 mg, or about 50 Mg/day to about 1000 Mg/day, for example about 5 Mg/day, about 10 Mg/day, about 15 Mg/day, about 20 Mg/day, about 25 Mg/day, about 30 Mg/day, about 35 Mg/day, about 40 Mg/day, about 45 Mg/day, about 50 Mg/day, about 55 Mg/day, about 60 Mg/day, about 65 Mg/day, about 70 Mg/day, about 75 Mg/day, about 80 Mg/day, about 85 Mg/day, about 90 Mg/day, about 95 Mg/day, about 100 Mg/day, about 105 Mg/day, about 1 10 Mg/day, about 1 15 Mg/day,
  • the pharmaceutical composition is in dry powder form suitable for administration by dry-powder inhaler. In some embodiments, the pharmaceutical composition is in powder form suitable for administration by metered-dose inhaler. In some embodiments, the pharmaceutical composition further comprises a propellant. In some embodiments, the propellant is 1 ,1 ,1 ,2-tetrafluoroethane.
  • the pharmaceutical composition is in a form suitable for administration by nebulizer.
  • the pharmaceutical composition is a solution comprising a solvent system.
  • the solvent system comprises an alcohol.
  • the solvent system does not include an alcohol.
  • the solvent system comprises a polyol.
  • the solvent system does not include a polyol.
  • the pharmaceutical composition is a suspension.
  • methods of the present disclosure further comprise determining a first forced expiratory volume (“FEV") value of the subject before administering the pharmaceutical composition; and determining a second FEV value of the subject after administering the pharmaceutical composition.
  • FEV forced expiratory volume
  • the second FEV value is greater than or substantially greater than the first FEV value.
  • the first and second FEV values are the volume of air the subject forcibly exhales in 0.5 seconds, 1 .0 second (i.e., "FEVi"), 2.0 seconds or 3.0 seconds.
  • methods of the present disclosure further comprise determining a first FEVi/FVC (forced vital capacity) value of the subject before administering the pharmaceutical composition, and determining a second FEVi/FVC value of the subject after administering the pharmaceutical composition.
  • the second FEV ⁇ FVC value is greater than or substantially greater than the first FEVi/FVC value.
  • the first FEVi/FVC value is no greater than about 70%.
  • the second FEVi/FVC value is greater than about 70%.
  • the first FEVi/FVC value is determined after administration of a bronchodilator medication.
  • the subject is male and the first FEVi/FVC value is no greater than about 88% of a predicted FEVi/FVC value for men having similar age and body composition of said subject. In some embodiments, the subject is female and the first FEVi/FVC value is no greater than about 89% of a predicted FEVi/FVC value for women having similar age and body composition of said subject.
  • the disease or disorder is selected from the group consisting of COPD or asthma. In some embodiments, the disease or disorder is COPD. In some embodiments, the disease or disorder is asthma.
  • methods according to the present disclosure further comprise administering (including co-administering) a second active agent.
  • the second active agent is selected from the group consisting of: short- acting bronchodilators (i.e. short-acting beta agonists), long-acting bronchodilators (i.e. long-acting beta agonists), phosphodiesterase-4 ("PDE4") inhibitors, corticosteroids, leukotriene receptor antagonists, expectorants and methylxanthines.
  • the second active agent is co-formulated with the pharmaceutical composition comprising 15-HEPE.
  • the second active agent is formulated separately and co-administered with the pharmaceutical composition comprising 15-HEPE.
  • the term "co-administer” includes administering the second active agent simultaneously, concomitantly, within 1 hour, within 2 hours, within 3 hours, 4 hours, within 5 hours, within 6 hours, within 7 hours, within 8 hours, within 9 hours, within 10 hours, within 1 1 hours, within 12 hours, within 13 hours, within 14 hours, within 15 hours, within 16 hours, within 17 hours, within 18 hours, within 19 hours, within 20 hours, within 21 hours, within 22 hours, within 23 hours, or within 24 hours of the pharmaceutical composition comprising 15-HEPE.
  • the method comprises administering a pharmaceutical composition as disclosed herein once per day, twice per day, three times per day, or more than three times per day.
  • the treated subject upon treatment in accordance with the present disclosure, for example over a period of about 1 to about 200 weeks, about 1 to about 100 weeks, about 1 to about 80 weeks, about 1 to about 50 weeks, about 1 to about 40 weeks, about 1 to about 20 weeks, about 1 to about 15 weeks, about 1 to about 12 weeks, about 1 to about 10 weeks, about 1 to about 5 weeks, about 1 to about 2 weeks or about 1 week, the treated subject exhibits an improvement in FEV value, an improvement in FCV value, or a combination thereof.
  • treating or “treatment” of a disease, disorder, or condition includes at least partially: (1 ) preventing the disease, disorder, or condition, i.e. causing the clinical symptoms of the disease, disorder, or condition not to develop in a mammal that is exposed to or predisposed to the disease, disorder, or condition but does not yet experience or display symptoms of the disease, disorder, or condition; (2) inhibiting the disease, disorder, or condition, i.e., arresting or reducing the development of the disease, disorder, or condition or its clinical symptoms; or (3) relieving the disease, disorder, or condition, i.e., causing regression of the disease, disorder, or condition or its clinical symptoms.
  • prevention in relation to a given disease or disorder means: preventing the onset of disease development if none had occurred, preventing the disease or disorder from occurring in a subject that may be predisposed to the disorder or disease but has not yet been diagnosed as having the disorder or disease, and/or preventing further disease/disorder development if already present.
  • an “effective amount,” as used herein, refers to the amount of an active composition that is required to confer a therapeutic effect on the subject.
  • a “therapeutically effective amount,” as used herein, refers to a sufficient amount of an agent or a compound being administered which will relieve to some extent one or more of the symptoms of the disease, disorder, or condition being treated. In some embodiments, the result is a reduction and/or alleviation of the signs, symptoms, or causes of a disease, or any other desired alteration of a biological system.
  • an “effective amount” for therapeutic uses is the amount of the composition including a compound as disclosed herein required to provide a clinically significant decrease in disease symptoms without undue adverse side effects.
  • an appropriate "effective amount” in any individual case is determined using techniques, such as a dose escalation study.
  • the term "therapeutically effective amount” includes, for example, a prophylactically effective amount.
  • an "effective amount” of a compound disclosed herein is an amount effective to achieve a desired pharmacologic effect or therapeutic improvement without undue adverse side effects.
  • an effective amount or “a therapeutically effective amount” varies from subject to subject, due to variation in metabolism, age, weight, general condition of the subject, the condition being treated, the severity of the condition being treated, and the judgment of the prescribing physician.
  • pharmaceutically acceptable in the present context means that the substance in question does not produce unacceptable toxicity to the subject or interaction with other components of the composition.
  • the present disclosure provides a method of treating, reducing the symptoms of, slowing progression of or promoting regression of a lung disease or disorder such as asthma or COPD.
  • the present disclosure provides a method of reducing or preventing side effects associated with administration of a second active agent.
  • Administration of certain second active agents disclosed herein have been associated with various intolerance symptoms, such as but not limited to: irritation of the oropharynx, mouth, mucus tissues, etc.; headache; nausea; upset stomach; severe allergic reactions (rash; hives; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue); blood in the urine; bloody vomit; diarrhea; dizziness; excitability; fast breathing; fast/irregular heartbeat; flushing; increased thirst or urination; irritability; muscle twitching; pounding in the chest; restlessness; seizures; stomach pain; trouble sleeping; and vomiting.
  • various intolerance symptoms such as but not limited to: irritation of the oropharynx, mouth, mucus tissues, etc.; headache; nausea; upset stomach; severe allergic reactions (rash; hives; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips,
  • a method of reducing side effects associated with administration of a second active agent as disclosed herein comprises discontinuing administration of a first pharmaceutical composition comprising the second active agent and administering to a subject a second pharmaceutical composition comprising 15-HEPE as disclosed herein.
  • the second pharmaceutical composition includes an amount of a second active agent that is less than the amount of the same second active agent in the first pharmaceutical composition.
  • the second pharmaceutical composition includes an amount of the second active agent that is about equal to or equal to the amount of that second active agent in the first pharmaceutical composition.
  • the second pharmaceutical composition includes an amount of the second active agent that is more than the amount of that second active agent in the first pharmaceutical composition.
  • the second pharmaceutical composition does not include the second active agent, essentially none of the second active agent, or substantially none of the second active agent.
  • Example 1 In vivo investigation of histamine-induced bronchoconstriction following chronic exposure to 15-HEPE in guinea pigs
  • the guinea pig is a reliable animal model in respiratory research due to their respiratory sensitivity and their expression of similar respiratory reactions to those observed in humans. Guinea pigs possess a well-developed bronchial smooth muscle compartment, integral to the purpose of this study.
  • test article was formulated using olive oil as the vehicle.
  • a low and a high dose of 15-HEPE 50 mg/kg and 500 mg/kg was formulated.
  • a 1 mg/ml stock solution of bambuterol was prepared in an aqueous solution, and was then mixed with olive oil in the gavage syringe for the vehicle effect.
  • the stock solution was stored at -20°C, but was used at room temperature and was considered stable for the duration of the experiment.
  • a 5 g/ml stock solution of histamine dihydrochloride (Sigma Aldrich) was prepared in a saline solution (0.9% NaCI). The stock solution was stored at 4°C. The expiration date was set at 14 days after preparation.
  • Guinea pigs were anesthetized with an intraperitoneal injection of urethane (1 .5 g/kg). A tracheotomy was performed and the animals were mechanically ventilated throughout the experiment. The ventilatory pressure was recorded and analyzed for signs of bronchospasm. A pulse oxymeter was attached to each animal's hind paw to obtain heart beat and oxygen saturation on the anaesthetized guinea pigs to continuously monitor the general condition of the animals during the surgical procedure.
  • a networked personal computer running Microsoft Windows was used for data acquisition.
  • the acquisition software was Axoscope 10.2 by Axon Instruments.
  • Axoscope 10.2 has been fully validated in the connected context in which it was used for this study.
  • Clampfit 10.2.0.14 analysis software (Axon Instruments), installed on networked personal computers running Microsoft Windows was used. Clampfit 10.2.0.14 has been fully validated in the connected context in which it was used.
  • the graphics software for illustrations is Microsoft Office Excel 2007 installed on networked personal computers running Microsoft Windows.
  • the ventilatory pressure was recorded continuously and was used to calculate the mean respiratory resistance.
  • One-way ANOVAs comparing pre- and post-exposure parameters across experimental groups. Statistical significance confirmed at p ⁇ 0.05.
  • Table 1 Changes in ventilator pressure (mm Hg) from baseline following nebulized histamine doses after seven consecutive days of gavage with vehicle.
  • Table 2 Changes in ventilator pressure (mm Hg) from baseline following nebulized histamine doses after seven consecutive days of gavage with bambuterol (0.27 mg/kg/day).
  • Table 3 Changes in ventilator pressure (mm Hg) from baseline following nebulized histamine doses after seven consecutive days of gavage with 15-HEPE (50 mg/kg/day).
  • Table 4 Changes in ventilator pressure (mm Hg) from baseline following nebulized histamine doses after seven consecutive days of gavage with 15-HEPE (500 mg/kg/day).

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Abstract

The disclosure provides compositions comprising 15-HEPE or derivatives thereof used singly or in combination with other active agents for the treatment and/or prevention of lung diseases and disorders such as asthma.

Description

PHARMACEUTICAL COMPOSITIONS COMPRISING 15-HEPE
AND METHODS OF TREATING ASTHMA AND LUNG DISORDERS USING SAME
CROSS-REFERENCE TO RELATED APPLICATION(S)
[0001] This application claims the benefit of U.S. Provisional Patent Application No. 61/926,052 entitled "PHARMACEUTICAL COMPOSITIONS COMPRISING 15-OHEPA AND METHODS OF TREATING ASTHMA AND LUNG DISORDERS USING SAME", which was filed on January 10, 2014, the contents of which are all incorporated by reference herein.
TECHNICAL FIELD
[0002] The disclosure generally relates to compositions comprising 15-HEPE used singly or in combination with other active agents for the treatment and/or prevention of asthma and lung disorders.
BACKGROUND
[0003] Lung diseases and disorders, such as asthma and COPD, affect millions world-wide.
[0004] Asthma is a chronic lung disease that inflames and narrows the airways. The narrowing of the airways is a result of muscle tightening as well as inflammation. The narrowing results in less air flowing into the lungs. Asthmatics tend to react strongly to airborne substances, leading to increases in mucus production; staring a chain reaction toward a full blown asthmatic attack. Symptoms include recurring periods of wheezing, chest tightness, shortness of breath, coughing and in extreme cases, can be fatal.
[0005] Asthma affects people of all ages, but it most often starts during childhood. According to one study by de Nijs et al. (Eur. Respir. Rev., vol. 22(127), pp. 44-52 (Mar. 1 , 2013)), approximately 95% of asthma patients have their first episode before the age of 6 years. Young males are consistently reported to have more prevalent wheeze and asthma than young females. However, at the age of 1 1 years, the prevalence of asthma in young males (7.7%) and young females (7.4%) is similar and after 16 years of age the disease is more common in females (6.2%) than in males (4.3%).
[0006] The predominant risk factors associated with childhood-onset asthma are genetic predisposition, a family history of allergy and asthma, viral respiratory infections, bacterial colonization, allergic sensitization and tobacco exposure.
[0007] Large, prospective follow-up studies have shown that early and persistent sensitizations to perennial allergens are a strong risk factor for asthma in childhood. Furthermore, childhood-onset asthma is typically associated with other atopic diseases, including allergic rhinitis and atopic dermatitis. Even at adult age the amounts of total and specific immunoglobulin IgE are higher in childhood-onset asthma than in adult-onset asthma. Thus, atopy and allergy seem to be closely linked to asthma starting in childhood.
[0008] Viral infections are another risk factor for developing early childhood asthma. Long-term follow-up studies have shown that wheezy episodes associated with rhinovirus infection are a strong predictor of asthma by the age of 6 years. However, studies have also reported that children with early wheezy symptoms and a predisposition to asthma and atopy are at increased risk of lower respiratory infection. Therefore, the direction of causality of viral infection and the development of asthma is still unclear.
[0009] Pre-natal and post-natal smoke exposure has been linked to asthma and other wheezy disorders, particularly in the first years of life. Also, exposure to traffic-related air pollution may cause asthma in children.
[0010] Daily inhaled corticosteroids are highly effective in improving asthma control in childhood-onset allergic asthma.
1 Adult-Onset Asthma
[0011] Adult-onset asthma, or late-onset asthma, is considered when asthma symptoms represent for the first time during adulthood. Several definitions of adult-onset asthma can be found in the literature. The age at diagnosis determining the term late-onset asthma varies from 12 years of age to >65 years of age. [0012] In contrast to childhood-onset asthma, less is known about the prevalence and factors associated with adult-onset asthma. Studies have shown that it mainly effects females, has a low remission rate and is less often associated with allergy and atopic diseases. In addition, many patients with adult-onset asthma have a poor prognosis, with a faster decline in lung function and more severe persistent airflow limitation. New-onset adult severe asthmatics have compromised lung function even if they have asthma of short duration, suggesting that significant loss of lung function occurs at or soon after the initial diagnosis. Still, adult-onset asthma is largely under investigated and far from completely understood.
2. Epidemiology of Adult-Onset Asthma
[0013] During the past 20 years, overall asthma prevalence has increased by 38%, in parallel with a similar increase in asthma-like symptoms and allergic rhinitis. Although prevalence rates have been studied more extensively in children, most studies confirm a real increase in asthma prevalence among adults as well. The estimated adult incidence of asthma from pooled general population studies appears to be 4.6 cases per 1 ,000 person- years in females and 3.6 in males, and there is a trend towards a higher incidence with age. The 5-year age- and sex-specific incidence of newly diagnosed asthma in adults >65 years of age is estimated to be 103 per 100,000 people, where two thirds of asthma deaths occur in people aged >65 years. Only one study investigated the long-term outcome of adult-onset asthma and changes in asthma severity over time. In this study, 95% of subjects still had an active asthma 5 years after diagnosis, and half of them had moderate-to-severe disease. Due to a relatively low remission rate, the prevalence of asthma in older adults (>65 years of age) has been reported to be as high as 10%, where females predominate the age group of 64-75 years. Still, these studies probably underestimate the true prevalence and incidence of asthma.
[0014] Besides atopy and atopic disorders, asthma can be a comorbid condition of other diseases. Asthma is a common comorbid factor in sickle cell disease (SCD). However, the incidence of asthma in SCD is much higher than expected compared to rates in the general population. Whether "asthma" in SCD is purely related to genetic and environmental factors or rather is the consequence of the underlying hemolytic and inflammatory state is a topic of recent debate. Regardless of the etiology, hypoxemia induced by bronchoconstriction and inflammation associated with asthma exacerbations will contribute to a cycle of sickling and subsequent complications of SCD. Recent studies confirm that asthma predisposes to complications of SCD such as pain crises, acute chest syndrome, and stroke, and is associated with increased mortality.
[0015] Chronic obstructive pulmonary disease (COPD) is the fourth leading cause of death in the United States, accounting for more than 1 10,000 deaths per year. COPD encompasses both chronic bronchitis and emphysema and is characterized by airway narrowing, air trapping, alveolar destruction, and excessive airway inflammation and oxidative stress. Cigarette smoke (CS) is the most common cause of COPD. In COPD there are marked increases in both inflammation and oxidative stress, which can be replicated in mice by exposing them to tobacco smoke.
[0016] Presently, there exist numerous regimens for the treatment of lung diseases and disorders, including short-acting bronchodilators (i.e. short-acting beta agonists), long- acting bronchodilators (i.e. long-acting beta agonists), phosphodiesterase-4 ("PDE4") inhibitors, corticosteroids, leukotriene receptor antagonists, expectorants and methylxanthines. However, such drugs are not always effective at reducing the symptoms, slowing the progression, or reversing the course of the clinical manifestation of the condition. Additionally, current regimens are limited in dose strength due to side effects and by inefficient delivery to a subject's lungs.
SUMMARY
[0017] The present disclosure provides compositions comprising fatty acid agents including, for example, 15-HEPE (also referred to as "15-OHEPA") used singly, in combination and/or in combination with a second active agent for treatment of lung diseases or disorders, such as asthma or COPD.
[0018] The present disclosure also provides methods for treating a lung disease or disorder mediated by 15-HEPE in a subject in need thereof comprising administering to subject a pharmaceutical composition comprising a therapeutically effective amount of 15- HEPE or combinations thereof. In some embodiments, the pharmaceutical composition comprises about 5 g to about 10,000 mg of 15-HEPE, for example about 50 g to about 4,000 mg of 15-HEPE. In some embodiments, the method comprises orally administering about 50 mg to about 4,000 mg of 15-HEPE to the subject per day.
[0019] The present disclosure also provides methods for treating a lung disease or disorder mediated by 15-HEPE in a subject in need thereof comprising administering to a subject a pharmaceutical composition comprising a therapeutically effective amount of 15- HEPE. In some embodiments, the pharmaceutical composition comprises about 5 g to about 10,000 mg of 15-HEPE, for example about 50 pg to about 4,000 mg of 15-HEPE. In some embodiments, the method comprises administering about 50 mg to about 4,000 mg of 15-HEPE to the subject per day.
[0020] In some embodiments, the pharmaceutical composition comprises one or more pharmaceutically acceptable excipients.
[0021] In some embodiments, the pharmaceutical composition comprises a second active agent. In some embodiments, the second active agent is one or more of: short- acting bronchodilators (i.e. short-acting beta agonists), long-acting bronchodilators (i.e. long-acting beta agonists), phosphodiesterase-4 ("PDE4") inhibitors, corticosteroids, leukotriene receptor antagonists, expectorants and methylxanthines.
[0022] In some embodiments, the step of administering comprises delivering the pharmaceutical composition to a lung of the subject by dry-powder inhaler. In some embodiments, the pharmaceutical composition is in dry powder form.
[0023] In some embodiments, the step of administering comprises delivering the pharmaceutical composition to a lung of the subject by metered dose inhaler. In some embodiments, the pharmaceutical composition is in powder form. In some embodiments, the pharmaceutical composition further comprises a propellant.
[0024] In some embodiments, the step of administering comprises delivering the pharmaceutical composition to a lung of the subject by nebulizer. In some embodiments, the pharmaceutical composition is a solution comprising a solvent system. In some embodiments, the solvent system comprises an alcohol and/or a polyol. In some embodiments, the solvent system does not include an alcohol or a polyol. In some embodiments, the pharmaceutical composition is a suspension.
[0025] In some embodiments, the step of administering the pharmaceutical composition comprises on oral dosage form. In some embodiments, compositions of the invention are in the form of solid dosage forms. Non-limiting examples of suitable solid dosage forms include tablets (e.g. suspension tablets, bite suspension tablets, rapid dispersion tablets, chewable tablets, melt tablets, effervescent tablets, bilayer tablets, etc), caplets, capsules (e.g. a soft or a hard gelatin capsule filled with solid and/or liquids), powder (e.g. a packaged powder, a dispensable powder or an effervescent powder), lozenges, sachets, cachets, troches, pellets, granules, microgranules, encapsulated microgranules, powder aerosol formulations, or any other solid dosage form reasonably adapted for oral administration.
[0026] In some embodiments, the pharmaceutical composition is formulated for intravenous or intramuscular injection by methods known in the art.
[0027] In some embodiments, the method comprises co-administering a pharmaceutical composition comprising 15-HEPE with a second active agent. In some embodiments, the second active agent is co-formulated with the pharmaceutical composition. In some embodiments, the second active agent is administered simultaneously, concomitantly, or within 1 to 24 hours of the pharmaceutical composition comprising 15-HEPE.
[0028] In one embodiment, the 15-HEPE is in the form of an ester. In another embodiment, the compositions comprise a Ci - C5 alkyl ester of 15-HEPE. In another embodiment, the compositions comprise a methyl ester, propyl ester, or butyl ester. In another embodiment the 15-HEPE is in the form of a pharmaceutically acceptable salt.
[0029] In another embodiment, the 15-HEPE comprises lithium, mono, di- or triglyceride or any other ester or 15-HEPE. In another embodiment, the 15-HEPE comprises salts, including but not limited to sodium, lysine, ornithine, piperazine or meglumine. In yet another embodiment, the 15-HEPE the free acid form of 15-HEPE. [0030] In one embodiment, 15-HEPE present in a composition of the invention comprises at least 90% by weight 15-HEPE (as the term "15-HEPE" is defined and exemplified herein). 15-HEPE compositions can comprise even higher purity compositions, for example at least 95% by weight 15-HEPE or at least 97% by weight 15- HEPE, wherein the 15-HEPE is any form of 15-HEPE as set forth herein.
[0031] In another embodiment, 15-HEPE is present in a composition of the invention in an amount of about 5 g to about 10,000 mg, about 25 mg to about 7500mg, 50 mg to about 5000 mg, about 75 mg to about 2500 mg, about 100 mg to about 1000 mg, or about 50 ig to about 1000 g, for example about 5 g, about 10 g, about 15 g, about 20 g, about 25 [ig, about 30 g, about 35 g, about 40 g, about 45 g, about 50 g, about 55 about 60 g, about 65 [ig, about 70 [ig, about 75 [ig, about 80 [ig, about 85 [ig, about 90 [ig, about 95 [ig, about 100 [ig, about 105 [ig, about 1 10 [ig, about 1 15 [ig, about 120 [ig, about 125 [ig, about 130 [ig, about 135 [ig, about 140 [ig, about 145 [ig, about 150 [ig, about 155 M9> about 160 M9> about 165 M9> about 170 M9> about 175 M9> about 180 pg about 185 M9> about 190 M9> about 195 M9> about 200 M9> about 205 M9> about 210 pg about 215 M9> about 220 M9> about 225 M9> about 230 M9> about 235 M9> about 240 Mg about 245 M9> about 250 M9> about 255 M9> about 260 M9> about 265 M9> about 270 Mg about 275 M9> about 280 M9> about 285 M9> about 290 M9> about 295 M9> about 300 Mg about 305 M9> about 310 M9> about 315 M9> about 320 M9> about 325 M9> about 330 Mg about 335 M9> about 340 M9> about 345 M9> about 350 M9> about 355 M9> about 360 Mg about 365 M9> about 370 M9> about 375 M9> about 380 M9> about 385 M9> about 390 Mg about 395 M9> about 400 M9> about 405 M9> about 410 M9> about 415 M9> about 420 Mg about 425 M9> about 430 M9> about 435 M9> about 440 M9> about 445 M9> about 450 Mg about 455 M9> about 460 M9> about 465 M9> about 470 M9> about 475 M9> about 480 Mg about 485 M9> about 490 M9> about 495 M9> about 500 M9> about 505 M9> about 510 Mg about 515 M9> about 520 M9> about 525 M9> about 530 M9> about 535 M9> about 540 Mg about 545 M9> about 550 M9> about 555 M9> about 560 M9> about 565 M9> about 570 Mg about 575 M9> about 580 M9> about 585 M9> about 590 M9> about 595 M9> about 600 Mg about 605 M9> about 610 M9> about 615 M9> about 620 M9> about 625 M9> about 630 Mg about 635 M9> about 640 M9> about 645 M9> about 650 M9> about 655 M9> about 660 Mg about 665 M9. about 670 M9. about 675 g, about 680 M9. about 685 M9. about 690 pg about 695 M9. about 700 M9> about 705 g, about 710 M9. about 715 M9> about 720 pg about 725 M9. about 730 M9> about 735 g, about 740 M9> about 745 M9> about 750 g about 755 M9. about 760 M9> about 765 g, about 770 M9> about 775 M9> about 780 g about 785 M9> about 790 M9> about 795 g, about 800 M9> about 805 M9> about 810 g about 815 M9> about 820 M9> about 825 g, about 830 M9> about 835 M9> about 840 g about 845 M9> about 850 M9> about 855 g, about 860 M9> about 865 M9> about 870 g about 875 M9> about 880 M9> about 885 g, about 890 M9> about 895 M9> about 900 pg about 905 M9> about 910 M9> about 915 g, about 920 M9> about 925 M9> about 930 pg about 935 M9> about 940 M9> about 945 g, about 950 M9> about 955 M9> about 960 pg about 965 M9> about 970 M9> about 975 g, about 980 M9> about 985 M9> about 990 pg about 995 pg, about 1000 pg, about 5 mg, about 10 mg, about 15 mg, about 20 mg, about 25mg, about 50mg, about 75 mg, about 100 mg, about 125 mg, about 150 mg, about 175 mg, about 200 mg, about 225 mg, about 250 mg, about 275 mg, about 300 mg, about 325 mg, about 350 mg, about 375 mg, about 400 mg, about 425 mg, about 450 mg, about 475 mg, about 500 mg, about 525 mg, about 550 mg, about 575 mg, about 600 mg, about 625 mg, about 650 mg, about 675 mg, about 700 mg, about 725 mg, about 750 mg, about 775 mg, about 800 mg, about 825 mg, about 850 mg, about 875 mg, about 900 mg, about 925 mg, about 950 mg, about 975 mg, about 1000 mg, about 1025 mg, about 1050 mg, about 1075 mg, about 1 100 mg, about 1025 mg, about 1050 mg, about 1075 mg, about 1200 mg, about 1225 mg, about 1250 mg, about 1275 mg, about 1300 mg, about 1325 mg, about 1350 mg, about 1375 mg, about 1400 mg, about 1425 mg, about 1450 mg, about 1475 mg, about 1500 mg, about 1525 mg, about 1550 mg, about 1575 mg, about 1600 mg, about 1625 mg, about 1650 mg, about 1675 mg, about 1700 mg, about 1725 mg, about 1750 mg, about 1775 mg, about 1800 mg, about 1825 mg, about 1850 mg, about 1875 mg, about 1900 mg, about 1925 mg, about 1950 mg, about 1975 mg, about 2000 mg, about 2025 mg, about 2050 mg, about 2075 mg, about 2100 mg, about 2125 mg, about 2150 mg, about 2175 mg, about 2200 mg, about 2225 mg, about 2250 mg, about 2275 mg, about 2300 mg, about 2325 mg, about 2350 mg, about 2375 mg, about 2400 mg, about 2425 mg, about 2450 mg, about 2475 mg, about 2500 mg about 2525 mg, about 2550 mg, about 2575 mg, about 2600 mg, about 2625 mg, about 2650 mg, about 2675 mg, about 2700 mg, about 2725 mg, about 2750 mg, about 2775 mg, about 2800 mg, about 2825 mg, about 2850 mg, about 2875 mg, about 2900 mg, about 2925 mg, about 2950 mg, about 2975 mg, about 3000 mg, about 3025 mg, about 3050 mg, about 3075 mg, about 3100 mg, about 3125 mg, about 3150 mg, about 3175 mg, about 3200 mg, about 3225 mg, about 3250 mg, about 3275 mg, about 3300 mg, about 3325 mg, about 3350 mg, about 3375 mg, about 3400 mg, about 3425 mg, about 3450 mg, about 3475 mg, about 3500 mg, about 3525 mg, about 3550 mg, about 3575 mg, about 3600 mg, about 3625 mg, about 3650 mg, about 3675 mg, about 3700 mg, about 3725 mg, about 3750 mg, about 3775 mg, about 3800 mg, about 3825 mg, about 3850 mg, about 3875 mg, about 3900 mg, about 3925 mg, about 3950 mg, about 3975 mg, about 4000 mg, about 4025 mg, about 4050 mg, about 4075 mg, about 4100 mg, about 4125 mg, about 4150 mg, about 4175 mg, about 4200 mg, about 4225 mg, about 4250 mg, about 4275 mg, about 4300 mg, about 4325 mg, about 4350 mg, about 4375 mg, about 4400 mg, about 4425 mg, about 4450 mg, about 4475 mg, about 4500 mg, about 4525 mg, about 4550 mg, about 4575 mg, about 4600 mg, about 4625 mg, about 4650 mg, about 4675 mg, about 4700 mg, about 4725 mg, about 4750 mg, about 4775 mg, about 4800 mg, about 4825 mg, about 4850 mg, about 4875 mg, about 4900 mg, about 4925 mg, about 4950 mg, about 4975 mg, about 5000 mg, about 5025 mg, about 5050 mg, about 5075 mg, about 5100 mg, about 5125 mg, about 5150 mg, about 5175 mg, about 5200 mg, about 5225 mg, about 5250 mg, about 5275 mg, about 5300 mg, about 5325 mg, about 5350 mg, about 5375 mg, about 5400 mg, about 5425 mg, about 5450 mg, about 5475 mg, about 5500 mg, about 5525 mg, about 5550 mg, about 5575 mg, about 5600 mg, about 5625 mg, about 5650 mg, about 5675 mg, about 5700 mg, about 5725 mg, about 5750 mg, about 5775 mg, about 5800 mg, about 5825 mg, about 5850 mg, about 5875 mg, about 5900 mg, about 5925 mg, about 5950 mg, about 5975 mg, about 6000 mg, about 6025 mg, about 6050 mg, about 6075 mg, about 6100 mg, about 6125 mg, about 6150 mg, about 6175 mg, about 6200 mg, about 6225 mg, about 6250 mg, about 6275 mg, about 6300 mg, about 6325 mg, about 6350 mg, about 6375 mg, about 6400 mg, about 6425 mg, about 6450 mg, about 6475 mg, about 6500 mg, about 6525 mg, about 6550 mg, about 6575 mg, about 6600 mg, about 6625 mg, about 6650 mg, about 6675 mg, about 6700 mg, about 6725 mg, about 6750 mg, about 6775 mg, about 6800 mg, about 6825 mg, about 6850 mg, about 6875 mg, about 6900 mg, about 6925 mg, about 6950 mg, about 6975 mg, about 7000 mg, about 7025 mg, about 7050 mg, about 7075 mg, about 7100 mg, about 7125 mg, about 7150 mg, about 7175 mg, about 7200 mg, about 7225 mg, about 7250 mg, about 7275 mg, about 7300 mg, about 7325 mg, about 7350 mg, about 7375 mg, about 7400 mg, about 7425 mg, about 7450 mg, about 7475 mg, about 7500 mg, about 7525 mg, about 7550 mg, about 7575 mg, about 7600 mg, about 7625 mg, about 7650 mg, about 7675 mg, about 7700 mg, about 7725 mg, about 7750 mg, about 7775 mg, about 7800 mg, about 7825 mg, about 7850 mg, about 7875 mg, about 7900 mg, about 7925 mg, about 7950 mg, about 7975 mg, about 8000 mg, about 8025 mg, about 8050 mg, about 8075 mg, about 8100 mg, about 8125 mg, about 8150 mg, about 8175 mg, about 8200 mg, about 8225 mg, about 8250 mg, about 8275 mg, about 8300 mg, about 8325 mg, about 8350 mg, about 8375 mg, about 8400 mg, about 8425 mg, about 8450 mg, about 8475 mg, about 8500 mg, about 8525 mg, about 8550 mg, about 8575 mg, about 8600 mg, about 8625 mg, about 8650 mg, about 8675 mg, about 8700 mg, about 8725 mg, about 8750 mg, about 8775 mg, about 8800 mg, about 8825 mg, about 8850 mg, about 8875 mg, about 8900 mg, about 8925 mg, about 8950 mg, about 8975 mg, about 9000 mg, about 9025 mg, about 9050 mg, about 9075 mg, about 9100 mg, about 9125 mg, about 9150 mg, about 9175 mg, about 9200 mg, about 9225 mg, about 9250 mg, about 9275 mg, about 9300 mg, about 9325 mg, about 9350 mg, about 9375 mg, about 9400 mg, about 9425 mg, about 9450 mg, about 9475 mg, about 9500 mg, about 9525 mg, about 9550 mg, about 9575 mg, about 9600 mg, about 9625 mg, about 9650 mg, about 9675 mg, about 9700 mg, about 9725 mg, about 9750 mg, about 9775 mg, about 9800 mg, about 9825 mg, about 9850 mg, about 9875 mg, about 9900 mg, about 9925 mg, about 9950 mg, about 9975 mg, or about 10,000 mg.
[0032] In one embodiment, a composition of the invention contains not more than about 10%, not more than about 9%, not more than about 8%, not more than about 7%, not more than about 6%, not more than about 5%, not more than about 4%, not more than about 3%, not more than about 2%, not more than about 1 %, or not more than about 0.5%, by weight of other omega-3 fatty acids such eicosapentaenoic acid, alpha linolenic acid, docosahexaenoic acid, docosapentaenoic acid or derivatives thereof.
[0033] In another embodiment, 15-HEPE represents at least about 60%, at least about 70%, at least about 80%, at least about 90%, at least about 95%, at least about 97%, at least about 98%, at least about 99%, or 100%, by weight, of all fatty acids present in a composition of the invention.
[0034] In one embodiment, the present disclosure provides a method for treating a lung disease or disorder comprising administering a pharmaceutical composition comprising 15-HEPE to a subject in need thereof.
[0035] These and other embodiments of the invention are described in further detail below.
BRIEF DESCRIPTION OF THE DRAWINGS
[0036] FIG. 1 shows ventilatory pressure (mm Hg) changes following exposition of nebulized histamine doses after seven consecutive days of gavage with vehicle.
[0037] FIG. 2 shows ventilatory pressure (mm Hg) changes following exposition of nebulized histamine doses after seven consecutive days of gavage with bambuterol at 0.27 mg/kg/day.
[0038] FIG. 3 shows ventilatory pressure (mm Hg) changes following exposition of nebulized histamine doses after seven consecutive days of gavage with 15-HEPE at 50 mg/kg/day.
[0039] FIG. 4 shows ventilatory pressure (mm Hg) changes following exposition of nebulized histamine doses after seven consecutive days of gavage with 15-HEPE at 500 mg/kg/day.
[0040] FIG. 5 shows ventilatory pressure (mm Hg) changes following exposition of nebulized histamine doses after seven consecutive days of gavage with vehicle, bambuterol (0.27mg/kg/day),OH-EPA (50 mg/kg/day) and OH-EPA (500mg/kg/day). DETAILED DESCRIPTION
[0041] The term "lung disease" as used herein refers to many disorders affecting the lungs, such as asthma, chronic obstructive pulmonary disease ("COPD"), infections like influenza, pneumonia and tuberculosis, lung cancer, and many other breathing problems.
[0042] The present disclosure provides compositions (e.g., pharmaceutical compositions) and formulations that comprise 15-HEPE. This agent has been found to improve lung ventilatory pressure in test animals when the animals were challenged with a bronchoconstrictor.
[0043] The present disclosure provides compositions comprising 15-HEPE in free acid or derivative form, used singly or in combination with additional active agents including, for example, short-acting bronchodilators (i.e. short-acting beta agonists), long- acting bronchodilators (i.e. long-acting beta agonists), phosphodiesterase-4 ("PDE4") inhibitors, corticosteroids, leukotriene receptor antagonists, expectorants and methylxanthines.
[0044] In some embodiments, the compositions comprise about 50 g/mL to about 1 ,000 g/mL of 15-HEPE or derivative thereof. Contemplated combinations include, without limitation, 15-HEPE and ipratropium, 15-HEPE and albuterol, 15-HEPE and levalbuterol, 15-HEPE with albuterol and levalbuterol, 15-HEPE and tiotropium, 15-HEPE and salmeterol, 15-HEPE and formoterol, 15-HEPE and aformoterol, 15-HEPE and prednisone, 15-HEPE and guaifenesin, 15-HEPE and aminophylline, 15-HEPE and theophylline, 15-HEPE and montelukast, 15-HEPE and zafirlukast, 15-HEPE and zileuton, 15-HEPE and pranlukast. In some embodiments, a composition comprising 15-HEPE includes a therapeutically effective amount of an additional active agent. In some embodiments, a composition comprising 15-HEPE includes less than a therapeutically effective amount of an additional active agent.
[0045] While the present disclosure is capable of being embodied in various forms, the description below of several embodiments is made with the understanding that the present disclosure is to be considered as an exemplification of the disclosure, and is not intended to limit the disclosure to the specific embodiments illustrated. Headings are provided for convenience only and are not to be construed to limit the disclosure in any manner. Embodiments illustrated under any heading may be combined with embodiments illustrated under any other heading.
[0046] The use of numerical values in the various quantitative values specified in this application, unless expressly indicated otherwise, are stated as approximations as though the minimum and maximum values within the stated ranges were both preceded by the word "about." Also, the disclosure of ranges is intended as a continuous range including every value between the minimum and maximum values recited as well as any ranges that can be formed by such values. Also disclosed herein are any and all ratios (and ranges of any such ratios) that can be formed by dividing a disclosed numeric value into any other disclosed numeric value. Accordingly, the skilled person will appreciate that many such ratios, ranges, and ranges of ratios can be unambiguously derived from the numerical values presented herein and in all instances such ratios, ranges, and ranges of ratios represent various embodiments of the present disclosure.
[0047] 15-Hydroxy-eicosa-5,8,1 1 ,13,17-pentaenoic acid ("15-HEPE") is a derivative of EPA. As used herein, the term "15-HEPE" refers to 15-HEPE in its free acid form (e.g, 15- hydroxy-eicosa-5,8,1 1 ,13,17-pentaenoic acid) and/or a pharmaceutically acceptable ester, derivative, conjugate or salt thereof, or mixtures of any of the foregoing. In some embodiments, the 15-HEPE is in the form of a Ci-4 alkyl ester such as methyl ester or ethyl ester form.
[0048] As used herein, the terms "15-HEPE derivative" and "derivative of 15-HEPE" refer to compounds formed from the chemical conversion of 15-HEPE including, without limitation, esters, derivatives, conjugates or salts thereof, or mixtures of any of the foregoing. One of skill in the art will readily recognize from the chemical structure and other properties whether a given compound is a 15-HEPE derivative.
[0049] In various embodiments, the invention provides pharmaceutical compositions, for example aerosolizable compositions, comprising of 15-HEPE.
[0050] In one embodiment, the present disclosure provides pharmaceutical compositions comprising, for example, an amount (e.g., a therapeutically effective amount) of 15-HEPE. In one embodiment, the pharmaceutical composition comprises about 50 pg/mL to about 1 ,000 pg/mL of 15-HEPE, for example 50 pg/mL, 60 pg/mL, 70 pg/mL, 80 pg/mL, 90 pg/mL, 100 pg/mL, 1 10 pg/mL, 120 pg/mL, 130 pg/mL, 140 pg/mL, 150 pg/mL, 160 pg/mL, 170 pg/mL, 180 pg/mL, 190 pg/mL, 200 pg/mL, 210 pg/mL, 220 pg/mL, 230 pg/mL, 240 pg/mL, 250 pg/mL, 260 pg/mL, 270 pg/mL, 280 pg/mL, 290 pg/mL, 300 pg/mL, 310 pg/mL, 320 pg/mL, 330 pg/mL, 340 pg/mL, 350 pg/mL, 360 pg/mL, 370 pg/mL, 380 pg/mL, 390 pg/mL, 400 pg/mL, 410 pg/mL, 420 pg/mL, 430 pg/mL, 440 pg/mL, 450 pg/mL, 460 pg/mL, 470 pg/mL, 480 pg/mL, 490 pg/mL, 500 pg/mL, 510 pg/mL, 520 pg/mL, 530 pg/mL, 540 pg/mL, 550 pg/mL, 560 pg/mL, 570 pg/mL, 580 pg/mL, 590 pg/mL, 600 pg/mL, 610 pg/mL, 620 pg/mL, 630 pg/mL, 640 pg/mL, 650 pg/mL, 660 pg/mL, 670 pg/mL, 680 pg/mL, 690 pg/mL, 700 pg/mL, 710 pg/mL, 720 pg/mL, 730 pg/mL, 740 pg/mL, 750 pg/mL, 760 pg/mL, 770 pg/mL, 780 pg/mL, 790 pg/mL, 800 pg/mL, 810 pg/mL, 820 pg/mL, 830 pg/mL, 840 pg/mL, 850 pg/mL, 860 pg/mL, 870 pg/mL, 880 pg/mL, 890 pg/mL, 900 pg/mL, 910 pg/mL, 920 pg/mL, 930 pg/mL, 940 pg/mL, 950 pg/mL, 960 pg/mL, 970 pg/mL, 980 pg/mL, 990 pg/mL, or 1 ,000 pg/mL of 15-HEPE.
[0051] In one embodiment, the pharmaceutical composition further comprises an additional active agent. In one embodiment, the pharmaceutical composition comprises an amount of the additional active agent that is less than the generally recognized therapeutically effective amount for that agent. In one embodiment, the pharmaceutical composition comprises an amount of the additional active agent that is equal to or greater than the generally recognized therapeutically effective amount for that agent. In one embodiment, the additional active agent has not previously been recognized as effective in the treatment of, including inhibition of, symptoms associated with lung diseases or disorders. In another embodiment, the additional active agent is approved for use in the treatment or prevention of a lung disease or disorder and/or the reduction of, including inhibition of, symptoms associated with a lung disease or disorder.
[0052] In one embodiment, the additional active agent is a short-acting bronchodilator. As used herein, the term "short-acting bronchodilator" refers to the class of compounds that are generally recommended for treatment of intermittent symptoms associated with a lung disease or disorder. For example and without limitation, short- acting bronchodilators include anticholinergics (e.g., ipratropium), beta-2-agonists (e.g., albuterol, levalbuterol), and combinations thereof (e.g., albuterol and ipratropium). In some embodiments, the method comprises administering the pharmaceutical composition comprising 15-HEPE and a short-acting bronchodilator in an amount sufficient to provide about 5 ig to about 2,000 [ig of short-acting bronchodilator to the subject per day, for example 5 [ig per day, 10 [ig per day, 18 [ig per day, 20 [ig per day, 25 [ig per day, 30 [ig per day, 35 [ig per day, 36 [ig per day, 40 [ig per day, 45 [ig per day, 50 [ig per day, 55 [ig per day, 60 [ig per day, 65 [ig per day, 70 [ig per day, 75 [ig per day, 80 [ig per day, 85 [ig per day, 90 [ig per day, 95 [ig per day, 100 [ig per day, 105 [ig per day, 1 10 g per day, 1 15 ig per day, 120 [ig per day, 125 [ig per day, 130 [ig per day, 135 [ig per day, 140 [ig per day, 145 [ig per day, 150 [ig per day, 155 [ig per day, 160 [ig per day, 165 [ig per day, 170 [ig per day, 175 [ig per day, 180 [ig per day, 185 [ig per day, 190 [ig per day, 195 [ig per day, 200 [ig per day, 205 [ig per day, 210 [ig per day, 215 [ig per day, 220 [ig per day, 225 [ig per day, 230 [ig per day, 235 [ig per day, 240 [ig per day, 245 [ig per day, 250 [ig per day, 255 [ig per day, 260 [ig per day, 265 [ig per day, 270 [ig per day, 275 g per day, 280 [ig per day, 285 [ig per day, 290 [ig per day, 295 [ig per day, 300 g per day, 305 [ig per day, 310 [ig per day, 315 [ig per day, 320 [ig per day, 325 g per day, 330 [ig per day, 335 [ig per day, 340 [ig per day, 345 [ig per day, 350 g per day, 355 [ig per day, 360 [ig per day, 365 [ig per day, 370 [ig per day, 375 g per day, 380 [ig per day, 385 [ig per day, 390 [ig per day, 395 [ig per day, 400 g per day, 405 [ig per day, 410 [ig per day, 415 [ig per day, 420 [ig per day, 425 g per day, 430 [ig per day, 435 [ig per day, 440 [ig per day, 445 [ig per day, 450 g per day, 455 [ig per day, 460 [ig per day, 465 [ig per day, 470 [ig per day, 475 g per day, 480 [ig per day, 485 [ig per day, 490 [ig per day, 495 [ig per day, 500 g per day, 525 [ig per day, 550 [ig per day, 575 [ig per day, 600 [ig per day, 625 g per day, 650 [ig per day, 675 [ig per day, 700 [ig per day, 725 [ig per day, 750 g per day, 775 [ig per day, 800 [ig per day, 825 [ig per day, 850 [ig per day, 875 g per day, 900 [ig per day, 925 [ig per day, 950 [ig per day, 975 [ig per day, 1 ,000 g per day, 1 ,025 [ig per day, 1 ,050 [ig per day, 1 ,075 [ig per day, 1 ,100 [ig per day, 1 ,125 [ig per day, 1 ,150 [ig per day, 1 ,175 [ig per day, 1 ,200 [ig per day, 1 ,225 [ig per day, 1 ,250 [ig per day, 1 ,275 [ig per day, 1 ,300 [ig per day, 1 ,325 [ig per day, 1 ,350 [ig per day, 1 ,375 [ig per day, 1 ,400 [ig per day, 1 ,425 [ig per day, 1 ,450 [ig per day, 1 ,475 [ig per day, 1 ,500 [ig per day, 1 ,525 [ig per day, 1 ,550 g per day, 1 ,575 g per day, 1 ,600 g per day, 1 ,625 g per day, 1 ,650 g per day, 1 ,675 g per day, 1 ,700 g per day, 1 ,725 g per day, 1 ,750 g per day, 1 ,775 g per day, 1 ,800 g per day, 1 ,825 g per day, 1 ,850 g per day, 1 ,875 g per day, 1 ,900 g per day, 1 ,925 g per day, 1 ,950 g per day, 1 ,975 g per day, or 2,000 g per day.
[0053] In one embodiment, the additional active agent is a long-acting bronchodilator. As used herein, the term "long-acting bronchodilator" refers to the class of compounds that are generally recommended for treatment of persistent symptoms associated with a lung disease or disorder. For example and without limitation, long-acting bronchodilators include anticholinergics (e.g., tiotropium), beta-2-agonists (e.g., salmeterol, formoterol, arformoterol), and combinations thereof. In some embodiments, the method comprises administering the pharmaceutical composition comprising 15-HEPE and a long-acting bronchodilator in an amount sufficient to provide about 5 g to about 100 g of long-acting bronchodilator to the subject per day, for example 5 g per day, 6 g per day, 7 g per day, 8 g per day, 9 g per day, 10 g per day, 1 1 g per day, 12 g per day, 13 g per day, 14 M9 per day, 15 M9 per day, 16 M9 per day, 17 M9 per day, 18 M9 per day, 19 M9 per day, 20 M9 per day, 21 M9 per day, 22 M9 per day, 23 M9 per day, 24 M9 per day, 25 M9 per day, 26 M9 per day, 27 M9 per day, 28 M9 per day, 29 M9 per day, 30 M9 per day, 31 M9 per day, 32 M9 per day, 33 M9 per day, 34 M9 per day, 35 M9 per day, 36 M9 per day, 37 M9 per day, 38 M9 per day, 39 M9 per day, 40 M9 per day, 41 M9 per day, 42 M9 per day, 43 M9 per day, 44 M9 per day, 45 M9 per day, 46 M9 per day, 47 M9 per day, 48 M9 per day, 49 M9 per day, 50 M9 per day, 51 M9 per day, 52 M9 per day, 53 M9 per day, 54 M9 per day, 55 M9 per day, 56 M9 per day, 57 M9 per day, 58 M9 per day, 59 M9 per day, 60 M9 per day, 61 M9 per day, 62 M9 per day, 63 M9 per day, 64 M9 per day, 65 M9 per day, 66 M9 per day, 67 M9 per day, 68 M9 per day, 69 M9 per day, 70 M9 per day, 71 M9 per day, 72 M9 per day, 73 M9 per day, 74 M9 per day, 75 M9 per day, 76 M9 per day, 77 M9 per day, 78 M9 per day, 79 M9 per day, 80 M9 per day, 81 M9 per day, 82 M9 per day, 83 M9 per day, 84 M9 per day, 85 M9 per day, 86 M9 per day, 87 M9 per day, 88 M9 per day, 89 M9 per day, 90 M9 per day, 91 M9 per day, 92 M9 per day, 93 M9 per day, 94 M9 per day, 95 M9 per day, 96 M9 per day, 97 M9 per day, 98 g per day, 99 g per day, or 100 g per day. [0054] In one embodiment, the additional active agent is a phosphodiesterase-4 ("PDE4") inhibitor. As used herein, the terms "phosphodiesterase-4 inhibitor" and "PDE4" inhibitor each refer to the class of compounds that are generally recommended to help prevent exacerbations associated with COPD (e.g., roflumilast). In some embodiments, the method comprises administering the pharmaceutical composition comprising 15-HEPE and a PDE4 inhibitor in an amount sufficient to provide about 250 [\g to about 1 ,000 [\g of PDE4 inhibitor to the subject per day, for example 250 [ig per day, 275 [ig per day, 300 [ig per day, 325 [ig per day, 350 [ig per day, 375 [ig per day, 400 [ig per day, 425 [ig per day, 450 ig per day, 475 [ig per day, 500 [ig per day, 525 [ig per day, 550 [ig per day, 575 [ig per day, 600 [ig per day, 625 [ig per day, 650 [ig per day, 675 [ig per day, 700 [ig per day, 725 ig per day, 750 [ig per day, 775 [ig per day, 800 [ig per day, 825 [ig per day, 850 [ig per day, 875 [ig per day, 900 [ig per day, 925 [ig per day, 950 [ig per day, 975 [ig per day, or 1 ,000 [ig per day. In one embodiment, the method comprises separately coadministering a PDE4 inhibitor and a pharmaceutical composition comprising 15-HEPE.
[0055] In one embodiment, the additional active agent is a corticosteroid. As used herein, the term "corticosteroid" refers to the class of compounds that are generally recommended to treat asthma, COPD exacerbation, stable symptoms of COPD, or progressing symptoms of COPD. For example and without limitation, corticosteroids include methylprednisolone, prednisolone, prednisone, beclomethasone, budesonide, flunisolide, fluticasone, mometasone, triamcinolone and combinations thereof. In some embodiments, the method comprises administering the pharmaceutical composition comprising 15-HEPE and a corticosteroid in an amount sufficient to provide about 50% to about 200% of the daily recommended corticosteroid dose to the subject per day, for example 50%, 55%, 60%, 65%, 70%, 75%, 80%, 85%, 90%, 95%, 100%, 105%, 1 10%, 1 15%, 120%, 125%, 130%, 135%, 140%, 145%, 150%, 155%, 160%, 165%, 170%, 175%, 180%, 185%, 190%, 195%, or 200% of the daily recommended corticosteroid dose per day. For avoidance of doubt, and not limiting in any way, the amount of a corticosteroid having a daily recommended dose of 40 mg per day to 80 mg per day could be present in a pharmaceutical formulation as disclosed herein (or administered according to a method disclosed herein) in an amount sufficient to provide from about 20 mg of the corticosteroid per day (i.e., 50% of the lowest recommended daily dose, 40 mg/day) to about 160 mg of the corticosteroid per day (i.e., 200% of the maximum daily recommended dose, 80 mg/day). In one embodiment, the corticosteroid is coformulated with the pharmaceutical composition comprising 15-HEPE. In one embodiment, the corticosteroid is in tablet or capsule form. In one embodiment, the method comprises separately co-administering a corticosteroid and a pharmaceutical composition comprising 15-HEPE.
[0056] In one embodiment, the additional active agent is an expectorant. As used herein, the term "expectorant" refers to the class of compounds that are generally recommended to help prevent mucus from sticking to the airways of the lungs (e.g., guaifenesin). In some embodiments, the method comprises administering the pharmaceutical composition comprising 15-HEPE and an expectorant in an amount sufficient to provide about 100 mg to about 3,000 mg of expectorant to the subject per day, for example 100 mg per day, 200 mg per day, 300 mg per day, 400 mg per day, 500 mg per day, 600 mg per day, 700 mg per day, 800 mg per day, 900 mg per day, 1 ,000 mg per day, 1 ,100 mg per day, 1 ,200 mg per day, 1 ,300 mg per day, 1 ,400 mg per day, 1 ,500 mg per day, 1 ,600 mg per day, 1 ,700 mg per day, 1 ,800 mg per day, 1 ,900 mg per day, 2,000 mg per day, 2,100 mg per day, 2,200 mg per day, 2,300 mg per day, 2,400 mg per day, 2,500 mg per day, 2,600 mg per day, 2,700 mg per day, 2,800 mg per day, 2,900 mg per day, or 3,000 mg per day. In one embodiment, the method comprises separately coadministering an expectorant and a pharmaceutical composition comprising 15-HEPE.
[0057] In one embodiment, the additional active agent is a methylxanthine. As used herein, the term "methylxanthine" refers to the class of compounds that are generally recommended for relaxing the airways in the lungs, increasing the strength of the diaphragm, stimulating the breathing control centers in the brain, and/or remove mucus from the lungs. For example and without limitation, methylxanthines include aminophylline, theophylline and combinations thereof. In some embodiments, the method comprises administering the pharmaceutical composition comprising 15-HEPE and a methylxanthine in an amount sufficient to provide about 100 mg to about 3,000 mg of methylxanthine to the subject per day, for example 100 mg per day, 200 mg per day, 300 mg per day, 400 mg per day, 500 mg per day, 600 mg per day, 700 mg per day, 800 mg per day, 900 mg per day, 1 ,000 mg per day, 1 ,100 mg per day, 1 ,200 mg per day, 1 ,300 mg per day, 1 ,400 mg per day, 1 ,500 mg per day, 1 ,600 mg per day, 1 ,700 mg per day, 1 ,800 mg per day, 1 ,900 mg per day, 2,000 mg per day, 2,100 mg per day, 2,200 mg per day, 2,300 mg per day, 2,400 mg per day, 2,500 mg per day, 2,600 mg per day, 2,700 mg per day, 2,800 mg per day, 2,900 mg per day, or 3,000 mg per day. In one embodiment, the method comprises separately co-administering an expectorant and a pharmaceutical composition comprising 15-HEPE. In some embodiments, the methylxanthine is administered separately as an intravenous solution. In some embodiments, a loading dose of the methylxanthine is also administered, with or without coadminstration of the 15- HEPE component.
[0058] Any pharmaceutically acceptable excipient known to those of skill in the art may be used in pharmaceutical compositions according to the present disclosure. Any excipient selected for use in the therapeutic compositions should be pharmaceutically acceptable and appropriate for the form in which the therapeutic composition will be used, e.g., aerosol, dry powder, capsule, tablet, cream, gel, milk, oil, lotion, and the like. Preferably, the excipient has an affinity for lung tissue, is well tolerated, and stable when used in an amount adequate to provide the desired consistency and ease of application. By way of example only, a pharmaceutical composition according to the present disclosure may comprise one or more of: propellants, preservatives, amphiphilic agents, surfactants, coloring agents, flavorants, buffers, antioxidants, stabilizers, fragrances, emollients, emulsifiers, thickeners, texturizers, and the like.
[0059] In one embodiment, the pharmaceutical composition comprises about 0.5 wt.% to about 5 wt.% of a surfactant, for example, about 0.5 wt.%, about 0.55 wt.%, about 0.6 wt.%, about 0.65 wt.%, about 0.7 wt.%, about 0.75 wt.%, about 0.8 wt.%, about 0.85 wt.%, about 0.9 wt.%, about 0.95 wt.%, about 1 wt.%, about 1 .05 wt.%, about 1 .1 wt.%, about 1 .15 wt.%, about 1 .2 wt.%, about 1 .25 wt.%, about 1 .3 wt.%, about 1 .35 wt.%, about 1 .4 wt.%, about 1 .45 wt.%, about 1 .5 wt.%, about 1 .55 wt.%, about 1 .6 wt.%, about 1 .65 wt.%, about 1 .7 wt.%, about 1 .75 wt.%, about 1 .8 wt.%, about 1 .85 wt.%, about 1 .9 wt.%, about 1 .95 wt.%, about 2 wt.%, about 2.05 wt.%, about 2.1 wt.%, about 2.15 wt.%, about 2.2 wt.%, about 2.25 wt.%, about 2.3 wt.%, about 2.35 wt.%, about 2.4 wt.%, about 2.45 wt.%, about 2.5 wt.%, about 2.55 wt.%, about 2.6 wt.%, about 2.65 wt.%, about 2.7 wt.%, about 2.75 wt.%, about 2.8 wt.%, about 2.85 wt.%, about 2.9 wt.%, about 2.95 wt.%, about 3 wt.%, about 3.05 wt.%, about 3.1 wt.%, about 3.15 wt.%, about 3.2 wt.%, about 3.25 wt.%, about 3.3 wt.%, about 3.35 wt.%, about 3.4 wt.%, about 3.45 wt.%, about 3.5 wt.%, about 3.55 wt.%, about 3.6 wt.%, about 3.65 wt.%, about 3.7 wt.%, about 3.75 wt.%, about 3.8 wt.%, about 3.85 wt.%, about 3.9 wt.%, about 3.95 wt.%, about 4 wt.%, about 4.05 wt.%, about 4.1 wt.%, about 4.15 wt.%, about 4.2 wt.%, about 4.25 wt.%, about 4.3 wt.%, about 4.35 wt.%, about 4.4 wt.%, about 4.45 wt.%, about 4.5 wt.%, about 4.55 wt.%, about 4.6 wt.%, about 4.65 wt.%, about 4.7 wt.%, about 4.75 wt.%, about 4.8 wt.%, about 4.85 wt.%, about 4.9 wt.%, about 4.95 wt.%, about 5 wt.% of the surfactant.
[0060] In one embodiment, the pharmaceutical composition comprises about 0.5 wt.% to about 5 wt.% of an emulsifier, for example, about 0.5 wt.%, about 0.55 wt.%, about 0.6 wt.%, about 0.65 wt.%, about 0.7 wt.%, about 0.75 wt.%, about 0.8 wt.%, about 0.85 wt.%, about 0.9 wt.%, about 0.95 wt.%, about 1 wt.%, about 1 .05 wt.%, about 1 .1 wt.%, about 1 .15 wt.%, about 1 .2 wt.%, about 1 .25 wt.%, about 1 .3 wt.%, about 1 .35 wt.%, about 1 .4 wt.%, about 1 .45 wt.%, about 1 .5 wt.%, about 1 .55 wt.%, about 1 .6 wt.%, about 1 .65 wt.%, about 1 .7 wt.%, about 1 .75 wt.%, about 1 .8 wt.%, about 1 .85 wt.%, about 1 .9 wt.%, about 1 .95 wt.%, about 2 wt.%, about 2.05 wt.%, about 2.1 wt.%, about 2.15 wt.%, about 2.2 wt.%, about 2.25 wt.%, about 2.3 wt.%, about 2.35 wt.%, about 2.4 wt.%, about 2.45 wt.%, about 2.5 wt.%, about 2.55 wt.%, about 2.6 wt.%, about 2.65 wt.%, about 2.7 wt.%, about 2.75 wt.%, about 2.8 wt.%, about 2.85 wt.%, about 2.9 wt.%, about 2.95 wt.%, about 3 wt.%, about 3.05 wt.%, about 3.1 wt.%, about 3.15 wt.%, about 3.2 wt.%, about 3.25 wt.%, about 3.3 wt.%, about 3.35 wt.%, about 3.4 wt.%, about 3.45 wt.%, about 3.5 wt.%, about 3.55 wt.%, about 3.6 wt.%, about 3.65 wt.%, about 3.7 wt.%, about 3.75 wt.%, about 3.8 wt.%, about 3.85 wt.%, about 3.9 wt.%, about 3.95 wt.%, about 4 wt.%, about 4.05 wt.%, about 4.1 wt.%, about 4.15 wt.%, about 4.2 wt.%, about 4.25 wt.%, about 4.3 wt.%, about 4.35 wt.%, about 4.4 wt.%, about 4.45 wt.%, about 4.5 wt.%, about 4.55 wt.%, about 4.6 wt.%, about 4.65 wt.%, about 4.7 wt.%, about 4.75 wt.%, about 4.8 wt.%, about 4.85 wt.%, about 4.9 wt.%, about 4.95 wt.%, about 5 wt.% of the emulsifier. [0061] In one embodiment, the pharmaceutical composition comprises a stabilizer. In one embodiment, the pharmaceutical composition comprises about 0.1 wt.% to about 5 wt.% of a stabilizer, for example about 0.1 wt.%, about 0.1 1 wt.%, about 0.12 wt.%, about 0.13 wt.%, about 0.14 wt.%, about 0.15 wt.%, about 0.16 wt.%, about 0.17 wt.%, about 0.18 wt.%, about 0.19 wt.%, about 0.2 wt.%, about 0.21 wt.%, about 0.22 wt.%, about 0.23 wt.%, about 0.24 wt.%, about 0.25 wt.%, about 0.26 wt.%, about 0.27 wt.%, about 0.28 wt.%, about 0.29 wt.%, about 0.3 wt.%, about 0.31 wt.%, about 0.32 wt.%, about 0.33 wt.%, about 0.34 wt.%, about 0.35 wt.%, about 0.36 wt.%, about 0.37 wt.%, about 0.38 wt.%, about 0.39 wt.%, about 0.4 wt.%, about 0.41 wt.%, about 0.42 wt.%, about 0.43 wt.%, about 0.44 wt.%, about 0.45 wt.%, about 0.46 wt.%, about 0.47 wt.%, about 0.48 wt.%, about 0.49 wt.%, about 0.5 wt.%, about 0.51 wt.%, about 0.52 wt.%, about 0.53 wt.%, about 0.54 wt.%, about 0.55 wt.%, about 0.56 wt.%, about 0.57 wt.%, about 0.58 wt.%, about 0.59 wt.%, about 0.6 wt.%, about 0.61 wt.%, about 0.62 wt.%, about 0.63 wt.%, about 0.64 wt.%, about 0.65 wt.%, about 0.66 wt.%, about 0.67 wt.%, about 0.68 wt.%, about 0.69 wt.%, about 0.7 wt.%, about 0.71 wt.%, about 0.72 wt.%, about 0.73 wt.%, about 0.74 wt.%, about 0.75 wt.%, about 0.76 wt.%, about 0.77 wt.%, about 0.78 wt.%, about 0.79 wt.%, about 0.8 wt.%, about 0.81 wt.%, about 0.82 wt.%, about 0.83 wt.%, about 0.84 wt.%, about 0.85 wt.%, about 0.86 wt.%, about 0.87 wt.%, about 0.88 wt.%, about 0.89 wt.%, about 0.9 wt.%, about 0.91 wt.%, about 0.92 wt.%, about 0.93 wt.%, about 0.94 wt.%, about 0.95 wt.%, about 0.96 wt.%, about 0.97 wt.%, about 0.98 wt.%, about 0.99 wt.%, about 1 wt.%, about 1 .01 wt.%, about 1 .02 wt.%, about 1 .03 wt.%, about 1 .04 wt.%, about 1 .05 wt.%, about 1 .06 wt.%, about 1 .07 wt.%, about 1 .08 wt.%, about 1 .09 wt.%, about 1 .1 wt.%, about 1 .1 1 wt.%, about 1 .12 wt.%, about 1 .13 wt.%, about 1 .14 wt.%, about 1 .15 wt.%, about 1 .16 wt.%, about 1 .17 wt.%, about 1 .18 wt.%, about 1 .19 wt.%, about 1 .2 wt.%, about 1 .21 wt.%, about 1 .22 wt.%, about 1 .23 wt.%, about 1 .24 wt.%, about 1 .25 wt.%, about 1 .26 wt.%, about 1 .27 wt.%, about 1 .28 wt.%, about 1 .29 wt.%, about 1 .3 wt.%, about 1 .31 wt.%, about 1 .32 wt.%, about 1 .33 wt.%, about 1 .34 wt.%, about 1 .35 wt.%, about 1 .36 wt.%, about 1 .37 wt.%, about 1 .38 wt.%, about 1 .39 wt.%, about 1 .4 wt.%, about 1 .41 wt.%, about 1 .42 wt.%, about 1 .43 wt.%, about 1 .44 wt.%, about 1 .45 wt.%, about 1 .46 wt.%, about 1 .47 wt.%, about 1 .48 wt.%, about 1 .49 wt.%, about 1 .5 wt.%, about 1 .51 wt.%, about 1 .52 wt.%, about 1 .53 wt.%, about 1 .54 wt.%, about 1 .55 wt.%, about 1 .56 wt.%, about 1 .57 wt.%, about 1 .58 wt.%, about 1 .59 wt.%, about 1 .6 wt.%, about 1 .61 wt.%, about 1 .62 wt.%, about 1 .63 wt.%, about 1 .64 wt.%, about 1 .65 wt.%, about 1 .66 wt.%, about 1 .67 wt.%, about 1 .68 wt.%, about 1 .69 wt.%, about 1 .7 wt.%, about 1 .71 wt.%, about 1 .72 wt.%, about 1 .73 wt.%, about 1 .74 wt.%, about 1 .75 wt.%, about 1 .76 wt.%, about 1 .77 wt.%, about 1 .78 wt.%, about 1 .79 wt.%, about 1 .8 wt.%, about 1 .81 wt.%, about 1 .82 wt.%, about 1 .83 wt.%, about 1 .84 wt.%, about 1 .85 wt.%, about 1 .86 wt.%, about 1 .87 wt.%, about 1 .88 wt.%, about 1 .89 wt.%, about 1 .9 wt.%, about 1 .91 wt.%, about 1 .92 wt.%, about 1 .93 wt.%, about 1 .94 wt.%, about 1 .95 wt.%, about 1 .96 wt.%, about 1 .97 wt.%, about 1 .98 wt.%, about 1 .99 wt.%, about 2 wt.%, about 2 wt.%, about 2.1 wt.%, about 2.2 wt.%, about 2.3 wt.%, about 2.4 wt.%, about 2.5 wt.%, about 2.6 wt.%, about 2.7 wt.%, about 2.8 wt.%, about 2.9 wt.%, about 3 wt.%, about 3.1 wt.%, about 3.2 wt.%, about 3.3 wt.%, about 3.4 wt.%, about 3.5 wt.%, about 3.6 wt.%, about 3.7 wt.%, about 3.8 wt.%, about 3.9 wt.%, about 4 wt.%, about 4.1 wt.%, about 4.2 wt.%, about 4.3 wt.%, about 4.4 wt.%, about 4.5 wt.%, about 4.6 wt.%, about 4.7 wt.%, about 4.8 wt.%, about 4.9 wt.%, or about 5 wt% of the stabilizer.
[0062] In one embodiment, the pharmaceutical composition comprises one or more antioxidants. In one embodiment, the pharmaceutical composition comprises about 0.01 wt.% to about 2 wt.% of an antioxidant, for example about 0.01 wt.%, about 0.02 wt.%, about 0.03 wt.%, about 0.04 wt.%, about 0.05 wt.%, about 0.06 wt.%, about 0.07 wt.%, about 0.08 wt.%, about 0.09 wt.%, about 0.1 wt.%, about 0.1 1 wt.%, about 0.12 wt.%, about 0.13 wt.%, about 0.14 wt.%, about 0.15 wt.%, about 0.16 wt.%, about 0.17 wt.%, about 0.18 wt.%, about 0.19 wt.%, about 0.2 wt.%, about 0.21 wt.%, about 0.22 wt.%, about 0.23 wt.%, about 0.24 wt.%, about 0.25 wt.%, about 0.26 wt.%, about 0.27 wt.%, about 0.28 wt.%, about 0.29 wt.%, about 0.3 wt.%, about 0.31 wt.%, about 0.32 wt.%, about 0.33 wt.%, about 0.34 wt.%, about 0.35 wt.%, about 0.36 wt.%, about 0.37 wt.%, about 0.38 wt.%, about 0.39 wt.%, about 0.4 wt.%, about 0.41 wt.%, about 0.42 wt.%, about 0.43 wt.%, about 0.44 wt.%, about 0.45 wt.%, about 0.46 wt.%, about 0.47 wt.%, about 0.48 wt.%, about 0.49 wt.%, about 0.5 wt.%, about 0.51 wt.%, about 0.52 wt.%, about 0.53 wt.%, about 0.54 wt.%, about 0.55 wt.%, about 0.56 wt.%, about 0.57 wt.%, about 0.58 wt.%, about 0.59 wt.%, about 0.6 wt.%, about 0.61 wt.%, about 0.62 wt.%, about 0.63 wt.%, about 0.64 wt.%, about 0.65 wt.%, about 0.66 wt.%, about 0.67 wt.%, about 0.68 wt.%, about 0.69 wt.%, about 0.7 wt.%, about 0.71 wt.%, about 0.72 wt.%, about 0.73 wt.%, about 0.74 wt.%, about 0.75 wt.%, about 0.76 wt.%, about 0.77 wt.%, about 0.78 wt.%, about 0.79 wt.%, about 0.8 wt.%, about 0.81 wt.%, about 0.82 wt.%, about 0.83 wt.%, about 0.84 wt.%, about 0.85 wt.%, about 0.86 wt.%, about 0.87 wt.%, about 0.88 wt.%, about 0.89 wt.%, about 0.9 wt.%, about 0.91 wt.%, about 0.92 wt.%, about 0.93 wt.%, about 0.94 wt.%, about 0.95 wt.%, about 0.96 wt.%, about 0.97 wt.%, about 0.98 wt.%, about 0.99 wt.%, about 1 wt.%, about 1 .1 wt.%, about 1 .2 wt.%, about 1 .3 wt.%, about 1 .4 wt.%, about 1 .5 wt.%, about 1 .6 wt.%, about 1 .7 wt.%, about 1 .8 wt.%, about 1 .9 wt.%, or about 2 wt.% of the one or more antioxidant.
[0063] In one embodiment, the pharmaceutical composition comprises a preservative. In one embodiment, the pharmaceutical composition comprises about 0.1 wt.% to about 5 wt.% of a preservative, for example about 0.1 wt.%, about 0.2 wt.%, about 0.3 wt.%, about 0.4 wt.%, about 0.5 wt.%, about 0.6 wt.%, about 0.7 wt.%, about 0.8 wt.%, about 0.9 wt.%, about 1 wt.%, about 1 .1 wt.%, about 1 .2 wt.%, about 1 .3 wt.%, about 1 .4 wt.%, about 1 .5 wt.%, about 1 .6 wt.%, about 1 .7 wt.%, about 1 .8 wt.%, about 1 .9 wt.%, about 2 wt.%, about 2.1 wt.%, about 2.2 wt.%, about 2.3 wt.%, about 2.4 wt.%, about 2.5 wt.%, about 2.6 wt.%, about 2.7 wt.%, about 2.8 wt.%, about 2.9 wt.%, about 3 wt.%, about 3.1 wt.%, about 3.2 wt.%, about 3.3 wt.%, about 3.4 wt.%, about 3.5 wt.%, about 3.6 wt.%, about 3.7 wt.%, about 3.8 wt.%, about 3.9 wt.%, about 4 wt.%, about 4.1 wt.%, about 4.2 wt.%, about 4.3 wt.%, about 4.4 wt.%, about 4.5 wt.%, about 4.6 wt.%, about 4.7 wt.%, about 4.8 wt.%, about 4.9 wt.%, or about 5 wt.% of a preservative.
[0064] In one embodiment, the pharmaceutical composition comprises: about 50 g/mL to about 4,000 mg/mL of one or more of 15-HEPE and optionally a second active agent.
[0065] A composition for use in accordance with the disclosure can be formulated as one or more dosage units. The terms "dose unit" and "dosage unit" herein refer to a portion of a pharmaceutical composition that contains an amount of a therapeutic agent suitable for a single administration to provide a therapeutic effect. Such dosage units may be administered one to a plurality (i.e. 1 to about 10, 1 to 8, 1 to 8, 1 to 4 or 1 to 2) of times per day, or as many times as needed to elicit a therapeutic response.
[0066] In one embodiment, a composition including, for example, a pharmaceutical composition, as disclosed herein is formulated as an aerosol, a capsule, a tablet or other oral dosage form..
[0067] Such formulations may be stable and comprise an amount (e.g., a therapeutically effective amount) of 15-HEPE, in combination with one or more second active agents selected from the group consisting of: short-acting bronchodilators (i.e. short- acting beta agonists), long-acting bronchodilators (i.e. long-acting beta agonists), phosphodiesterase-4 ("PDE4") inhibitors, corticosteroids, leukotriene receptor antagonists, expectorants and methylxanthines. Pharmacokinetics/Pharmacodynamics
[0068] The pharmacokinetics and/or pharmacodynamics of the compositions comprising 15-HEPE as disclosed herein may be determined by any method known in the art.
[0069] In an embodiment, the pharmacodynamics of a composition comprising 15- HEPE as disclosed herein may be examined using a model of a lung disease or disorder. In a more detailed embodiment, the effects of a composition comprising a vehicle, a positive control or 15-HEPE on ventilator pressure in histamine challenged guinea pigs serves as a model for the pharmacodynamics in asthma. In an exemplary method, guinea pigs are first dosed with compositions comprising a vehicle, a positive control or 15-HEPE for seven days. The treated guinea pigs can then be anesthetized and exposed to a nebulized bronchoconstictor to determine if 15-HEPE can reduce the increase in ventilatory pressure induced by a bronchoconstrictor. This serves as an effective model for asthma and other lung diseases.
2. Methods of Treatment of Diseases and/or Disorders
[0070] The compositions and formulations disclosed herein may be used in the treatment of diseases and/or disorders including, for example, lung diseases and/or disorders such as asthma or COPD. [0071 ] In some embodiments, compositions of the invention are in the form of solid dosage forms for oral delivery. Non-limiting examples of suitable solid dosage forms include tablets (e.g. suspension tablets, bite suspension tablets, rapid dispersion tablets, chewable tablets, melt tablets, effervescent tablets, bilayer tablets, etc), caplets, capsules (e.g. a soft or a hard gelatin capsule filled with solid and/or liquids), powder (e.g. a packaged powder, a dispensable powder or an effervescent powder), lozenges, sachets, cachets, troches, pellets, granules, microgranules, encapsulated microgranules, powder aerosol formulations, or any other solid dosage form reasonably adapted for oral administration.
[0072] In another embodiment, 15-HEPE is present in a composition of the invention in an amount of about 5 [\g to about 10,000 mg, about 25 mg to about 7500mg, 50 mg to about 5000 mg, about 75 mg to about 2500 mg, about 100 mg to about 1000 mg, or about 50 \ig to about 1000 \ig, for example about 5 \ig, about 10 \ig, about 15 \ig, about 20 \ig, about 25 [ig, about 30 \ig, about 35 \ig, about 40 \ig, about 45 \ig, about 50 \ig, about 55 about 60 \ig, about 65 [ig, about 70 [ig, about 75 [ig, about 80 [ig, about 85 [ig, about 90 [ig, about 95 [ig, about 100 [ig, about 105 [ig, about 1 10 [ig, about 1 15 [ig, about 120 [ig, about 125 [ig, about 130 [ig, about 135 [ig, about 140 [ig, about 145 [ig, about 150 [ig, about 155 M9. about 160 M9. about 165 M9. about 170 M9> about 175 M9> about 180 \ig about 185 M9. about 190 M9> about 195 M9> about 200 M9> about 205 M9> about 210 pg about 215 M9. about 220 M9> about 225 M9> about 230 M9> about 235 M9> about 240 [ig about 245 M9. about 250 M9> about 255 M9> about 260 M9> about 265 M9> about 270 pg about 275 M9> about 280 M9> about 285 M9> about 290 M9> about 295 M9> about 300 pg about 305 M9> about 310 M9> about 315 M9> about 320 M9> about 325 M9> about 330 pg about 335 M9> about 340 M9> about 345 M9> about 350 M9> about 355 M9> about 360 pg about 365 M9> about 370 M9> about 375 M9> about 380 M9> about 385 M9> about 390 pg about 395 M9> about 400 M9> about 405 M9> about 410 M9> about 415 M9> about 420 g about 425 M9> about 430 M9> about 435 M9> about 440 M9> about 445 M9> about 450 g about 455 M9> about 460 M9> about 465 M9> about 470 M9> about 475 M9> about 480 g about 485 M9> about 490 M9> about 495 M9> about 500 M9> about 505 M9> about 510 g about 515 M9> about 520 M9> about 525 M9> about 530 M9> about 535 M9> about 540 g about 545 M9> about 550 M9> about 555 M9> about 560 M9> about 565 M9> about 570 pg about 575 M9> about 580 M9> about 585 M9> about 590 M9> about 595 M9> about 600 pg about 605 M9> about 610 M9> about 615 M9> about 620 M9> about 625 M9> about 630 Mg about 635 M9> about 640 M9> about 645 M9> about 650 M9> about 655 M9> about 660 Mg about 665 M9> about 670 M9> about 675 M9> about 680 M9> about 685 M9> about 690 Mg about 695 M9> about 700 M9> about 705 M9> about 710 M9> about 715 M9> about 720 Mg about 725 M9> about 730 M9> about 735 M9> about 740 M9> about 745 M9> about 750 Mg about 755 M9> about 760 M9> about 765 M9> about 770 M9> about 775 M9> about 780 Mg about 785 M9> about 790 M9> about 795 M9> about 800 M9> about 805 M9> about 810 Mg about 815 M9> about 820 M9> about 825 M9> about 830 M9> about 835 M9> about 840 Mg about 845 M9> about 850 M9> about 855 M9> about 860 M9> about 865 M9> about 870 Mg about 875 M9> about 880 M9> about 885 M9> about 890 M9> about 895 M9> about 900 Mg about 905 M9> about 910 M9> about 915 M9> about 920 M9> about 925 M9> about 930 Mg about 935 M9> about 940 M9> about 945 M9> about 950 M9> about 955 M9> about 960 Mg about 965 M9> about 970 M9> about 975 M9> about 980 M9> about 985 M9> about 990 Mg about 995 Mg, about 1000 Mg> about 5 mg, about 10 mg, about 15 mg, about 20 mg, about 25mg, about 50mg, about 75 mg, about 100 mg, about 125 mg, about 150 mg, about 175 mg, about 200 mg, about 225 mg, about 250 mg, about 275 mg, about 300 mg, about 325 mg, about 350 mg, about 375 mg, about 400 mg, about 425 mg, about 450 mg, about 475 mg, about 500 mg, about 525 mg, about 550 mg, about 575 mg, about 600 mg, about 625 mg, about 650 mg, about 675 mg, about 700 mg, about 725 mg, about 750 mg, about 775 mg, about 800 mg, about 825 mg, about 850 mg, about 875 mg, about 900 mg, about 925 mg, about 950 mg, about 975 mg, about 1000 mg, about 1025 mg, about 1050 mg, about 1075 mg, about 1 100 mg, about 1025 mg, about 1050 mg, about 1075 mg, about 1200 mg, about 1225 mg, about 1250 mg, about 1275 mg, about 1300 mg, about 1325 mg, about 1350 mg, about 1375 mg, about 1400 mg, about 1425 mg, about 1450 mg, about 1475 mg, about 1500 mg, about 1525 mg, about 1550 mg, about 1575 mg, about 1600 mg, about 1625 mg, about 1650 mg, about 1675 mg, about 1700 mg, about 1725 mg, about 1750 mg, about 1775 mg, about 1800 mg, about 1825 mg, about 1850 mg, about 1875 mg, about 1900 mg, about 1925 mg, about 1950 mg, about 1975 mg, about 2000 mg, about 2025 mg, about 2050 mg, about 2075 mg, about 2100 mg, about 2125 mg, about 2150 mg, about 2175 mg, about 2200 mg, about 2225 mg, about 2250 mg, about 2275 mg, about 2300 mg, about 2325 mg, about 2350 mg, about 2375 mg, about 2400 mg, about 2425 mg, about 2450 mg, about 2475 mg, about 2500 mg about 2525 mg, about 2550 mg, about 2575 mg, about 2600 mg, about 2625 mg, about 2650 mg, about 2675 mg, about 2700 mg, about 2725 mg, about 2750 mg, about 2775 mg, about 2800 mg, about 2825 mg, about 2850 mg, about 2875 mg, about 2900 mg, about 2925 mg, about 2950 mg, about 2975 mg, about 3000 mg, about 3025 mg, about 3050 mg, about 3075 mg, about 3100 mg, about 3125 mg, about 3150 mg, about 3175 mg, about 3200 mg, about 3225 mg, about 3250 mg, about 3275 mg, about 3300 mg, about 3325 mg, about 3350 mg, about 3375 mg, about 3400 mg, about 3425 mg, about 3450 mg, about 3475 mg, about 3500 mg, about 3525 mg, about 3550 mg, about 3575 mg, about 3600 mg, about 3625 mg, about 3650 mg, about 3675 mg, about 3700 mg, about 3725 mg, about 3750 mg, about 3775 mg, about 3800 mg, about 3825 mg, about 3850 mg, about 3875 mg, about 3900 mg, about 3925 mg, about 3950 mg, about 3975 mg, about 4000 mg, about 4025 mg, about 4050 mg, about 4075 mg, about 4100 mg, about 4125 mg, about 4150 mg, about 4175 mg, about 4200 mg, about 4225 mg, about 4250 mg, about 4275 mg, about 4300 mg, about 4325 mg, about 4350 mg, about 4375 mg, about 4400 mg, about 4425 mg, about 4450 mg, about 4475 mg, about 4500 mg, about 4525 mg, about 4550 mg, about 4575 mg, about 4600 mg, about 4625 mg, about 4650 mg, about 4675 mg, about 4700 mg, about 4725 mg, about 4750 mg, about 4775 mg, about 4800 mg, about 4825 mg, about 4850 mg, about 4875 mg, about 4900 mg, about 4925 mg, about 4950 mg, about 4975 mg, about 5000 mg, about 5025 mg, about 5050 mg, about 5075 mg, about 5100 mg, about 5125 mg, about 5150 mg, about 5175 mg, about 5200 mg, about 5225 mg, about 5250 mg, about 5275 mg, about 5300 mg, about 5325 mg, about 5350 mg, about 5375 mg, about 5400 mg, about 5425 mg, about 5450 mg, about 5475 mg, about 5500 mg, about 5525 mg, about 5550 mg, about 5575 mg, about 5600 mg, about 5625 mg, about 5650 mg, about 5675 mg, about 5700 mg, about 5725 mg, about 5750 mg, about 5775 mg, about 5800 mg, about 5825 mg, about 5850 mg, about 5875 mg, about 5900 mg, about 5925 mg, about 5950 mg, about 5975 mg, about 6000 mg, about 6025 mg, about 6050 mg, about 6075 mg, about 6100 mg, about 6125 mg, about 6150 mg, about 6175 mg, about 6200 mg, about 6225 mg, about 6250 mg, about 6275 mg, about 6300 mg, about 6325 mg, about 6350 mg, about 6375 mg, about 6400 mg, about 6425 mg, about 6450 mg, about 6475 mg, about 6500 mg, about 6525 mg, about 6550 mg, about 6575 mg, about 6600 mg, about 6625 mg, about 6650 mg, about 6675 mg, about 6700 mg, about 6725 mg, about 6750 mg, about 6775 mg, about 6800 mg, about 6825 mg, about 6850 mg, about 6875 mg, about 6900 mg, about 6925 mg, about 6950 mg, about 6975 mg, about 7000 mg, about 7025 mg, about 7050 mg, about 7075 mg, about 7100 mg, about 7125 mg, about 7150 mg, about 7175 mg, about 7200 mg, about 7225 mg, about 7250 mg, about 7275 mg, about 7300 mg, about 7325 mg, about 7350 mg, about 7375 mg, about 7400 mg, about 7425 mg, about 7450 mg, about 7475 mg, about 7500 mg, about 7525 mg, about 7550 mg, about 7575 mg, about 7600 mg, about 7625 mg, about 7650 mg, about 7675 mg, about 7700 mg, about 7725 mg, about 7750 mg, about 7775 mg, about 7800 mg, about 7825 mg, about 7850 mg, about 7875 mg, about 7900 mg, about 7925 mg, about 7950 mg, about 7975 mg, about 8000 mg, about 8025 mg, about 8050 mg, about 8075 mg, about 8100 mg, about 8125 mg, about 8150 mg, about 8175 mg, about 8200 mg, about 8225 mg, about 8250 mg, about 8275 mg, about 8300 mg, about 8325 mg, about 8350 mg, about 8375 mg, about 8400 mg, about 8425 mg, about 8450 mg, about 8475 mg, about 8500 mg, about 8525 mg, about 8550 mg, about 8575 mg, about 8600 mg, about 8625 mg, about 8650 mg, about 8675 mg, about 8700 mg, about 8725 mg, about 8750 mg, about 8775 mg, about 8800 mg, about 8825 mg, about 8850 mg, about 8875 mg, about 8900 mg, about 8925 mg, about 8950 mg, about 8975 mg, about 9000 mg, about 9025 mg, about 9050 mg, about 9075 mg, about 9100 mg, about 9125 mg, about 9150 mg, about 9175 mg, about 9200 mg, about 9225 mg, about 9250 mg, about 9275 mg, about 9300 mg, about 9325 mg, about 9350 mg, about 9375 mg, about 9400 mg, about 9425 mg, about 9450 mg, about 9475 mg, about 9500 mg, about 9525 mg, about 9550 mg, about 9575 mg, about 9600 mg, about 9625 mg, about 9650 mg, about 9675 mg, about 9700 mg, about 9725 mg, about 9750 mg, about 9775 mg, about 9800 mg, about 9825 mg, about 9850 mg, about 9875 mg, about 9900 mg, about 9925 mg, about 9950 mg, about 9975 mg, or about 10,000 mg. [0073] In one embodiment, a composition of the invention contains not more than about 10%, not more than about 9%, not more than about 8%, not more than about 7%, not more than about 6%, not more than about 5%, not more than about 4%, not more than about 3%, not more than about 2%, not more than about 1%, or not more than about 0.5%, by weight of other omega-3 fatty acids such eicosapentaenoic acid, alpha linolenic acid, docosahexaenoic acid, docosapentaenoic acid or derivatives thereof.
[0074] In another embodiment, 15-HEPE represents at least about 60%, at least about 70%, at least about 80%, at least about 90%, at least about 95%, at least about 97%, at least about 98%, at least about 99%, or 100%, by weight, of all fatty acids present in a composition of the invention.
[0075] In some embodiments, the present disclosure provides a method for treating a disease or disorder mediated by 15-HEPE comprising administering a pharmaceutical composition comprising 15-HEPE to a subject in need thereof. In some embodiments, the pharmaceutical composition comprises about 50 g/mL to about 1,000 g/mL of 15-HEPE, for example about 50 pg/mL, about 60 pg/mL, about 70 pg/mL, about 80 pg/mL, about 90 g/mL, about 100 g/mL, about 110 g/mL, about 120 g/mL, about 130 g/mL, about 140 g/mL, about 150 g/mL, about 160 g/mL, about 170 g/mL, about 180 g/mL, about 190 g/mL, about 200 g/mL, about 210 g/mL, about 220 g/mL, about 230 g/mL, about 240 g/mL, about 250 g/mL, about 260 g/mL, about 270 g/mL, about 280 g/mL, about 290 g/mL, about 300 g/mL, about 310 g/mL, about 320 g/mL, about 330 g/mL, about 340 g/mL, about 350 g/mL, about 360 g/mL, about 370 g/mL, about 380 g/mL, about 390 g/mL, about 400 g/mL, about 410 g/mL, about 420 g/mL, about 430 g/mL, about 440 g/mL, about 450 g/mL, about 460 g/mL, about 470 g/mL, about 480 g/mL, about 490 g/mL, about 500 g/mL, about 510 g/mL, about 520 g/mL, about 530 g/mL, about 540 g/mL, about 550 g/mL, about 560 g/mL, about 570 g/mL, about 580 g/mL, about 590 g/mL, about 600 g/mL, about 610 g/mL, about 620 g/mL, about 630 g/mL, about 640 g/mL, about 650 g/mL, about 660 g/mL, about 670 g/mL, about 680 g/mL, about 690 g/mL, about 700 g/mL, about 710 g/mL, about 720 g/mL, about 730 g/mL, about 740 g/mL, about 750 g/mL, about 760 g/mL, about 770 g/mL, about 780 g/mL, about 790 g/mL, about 800 g/mL, about 810 g/mL, about 820 g/mL, about 830 g/mL, about 840 Mg/mL, about 850 Mg/mL, about 860 Mg/mL, about 870 Mg/mL, about 880 Mg/mL, about 890 Mg/mL, about 900 Mg/mL, about 910 Mg/mL, about 920 Mg/mL, about 930 Mg/mL, about 940 Mg/mL, about 950 Mg/mL, about 960 Mg/mL, about 970 Mg/mL, about 980 Mg/mL, about 990 Mg/mL, or about 1000 Mg/mL. In some embodiments, the subject is administered about 5 Mg to about 4,000 mg of 15-HEPE per day, for example about 5 Mg/day to about 10,000 mg, about 25 mg to about 7500mg, 50 mg to about 5000 mg, about 75 mg to about 2500 mg, about 100 mg to about 1000 mg, or about 50 Mg/day to about 1000 Mg/day, for example about 5 Mg/day, about 10 Mg/day, about 15 Mg/day, about 20 Mg/day, about 25 Mg/day, about 30 Mg/day, about 35 Mg/day, about 40 Mg/day, about 45 Mg/day, about 50 Mg/day, about 55 Mg/day, about 60 Mg/day, about 65 Mg/day, about 70 Mg/day, about 75 Mg/day, about 80 Mg/day, about 85 Mg/day, about 90 Mg/day, about 95 Mg/day, about 100 Mg/day, about 105 Mg/day, about 1 10 Mg/day, about 1 15 Mg/day, about 120 Mg/day, about 125 Mg/day, about 130 Mg/day, about 135 Mg/day, about 140 Mg/day, about 145 Mg/day, about 150 Mg/day, about 155 Mg/day, about 160 Mg/day, about 165 Mg/day, about 170 Mg/day, about 175 Mg/day, about 180 Mg/day, about 185 Mg/day, about 190 Mg/day, about 195 Mg/day, about 200 Mg/day, about 205 Mg/day, about 210 Mg/day, about 215 Mg/day, about 220 Mg/day, about 225 Mg/day, about 230 Mg/day, about 235 Mg/day, about 240 Mg/day, about 245 Mg/day, about 250 Mg/day, about 255 Mg/day, about 260 Mg/day, about 265 Mg/day, about 270 Mg/day, about 275 Mg/day, about 280 Mg/day, about 285 Mg/day, about 290 Mg/day, about 295 Mg/day, about 300 Mg/day, about 305 Mg/day, about 310 Mg/day, about 315 Mg/day, about 320 Mg/day, about 325 Mg/day, about 330 Mg/day, about 335 Mg/day, about 340 Mg/day, about 345 Mg/day, about 350 Mg/day, about 355 Mg/day, about 360 Mg/day, about 365 Mg/day, about 370 Mg/day, about 375 Mg/day, about 380 Mg/day, about 385 Mg/day, about 390 Mg/day, about 395 Mg/day, about 400 Mg/day, about 405 Mg/day, about 410 Mg/day, about 415 Mg/day, about 420 Mg/day, about 425 Mg/day, about 430 Mg/day, about 435 Mg/day, about 440 Mg/day, about 445 Mg/day, about 450 Mg/day, about 455 Mg/day, about 460 Mg/day, about 465 Mg/day, about 470 Mg/day, about 475 Mg/day, about 480 Mg/day, about 485 Mg/day, about 490 Mg/day, about 495 Mg/day, about 500 Mg/day, about 505 Mg/day, about 510 Mg/day, about 515 Mg/day, about 520 Mg/day, about 525 Mg/day, about 530 Mg/day, about 535 Mg/day, about 540 Mg/day, about 545 Mg/day, about 550 Mg/day, about 555 Mg/day, about 560 Mg/day, about 565 Mg/day, about 570 pg/day, about 575 pg/day, about 580 pg/day, about 585 pg/day, about 590 Mg/day, about 595 pg/day, about 600 pg/day, about 605 pg/day, about 610 pg/day, about 615 Mg/day, about 620 pg/day, about 625 pg/day, about 630 pg/day, about 635 pg/day, about 640 pg/day, about 645 pg/day, about 650 pg/day, about 655 pg/day, about 660 Mg/day, about 665 pg/day, about 670 pg/day, about 675 pg/day, about 680 pg/day, about 685 Mg/day, about 690 pg/day, about 695 pg/day, about 700 pg/day, about 705 pg/day, about 710 Mg/day, about 715 pg/day, about 720 pg/day, about 725 pg/day, about 730 Mg/day, about 735 pg/day, about 740 pg/day, about 745 pg/day, about 750 pg/day, about 755 Mg/day, about 760 pg/day, about 765 pg/day, about 770 pg/day, about 775 pg/day, about 780 pg/day, about 785 pg/day, about 790 pg/day, about 795 pg/day, about 800 Mg/day, about 805 pg/day, about 810 pg/day, about 815 pg/day, about 820 pg/day, about 825 Mg/day, about 830 pg/day, about 835 pg/day, about 840 pg/day, about 845 pg/day, about 850 pg/day, about 855 pg/day, about 860 pg/day, about 865 pg/day, about 870 Mg/day, about 875 pg/day, about 880 pg/day, about 885 pg/day, about 890 pg/day, about 895 Mg/day, about 900 pg/day, about 905 pg/day, about 910 pg/day, about 915 pg/day, about 920 pg/day, about 925 pg/day, about 930 pg/day, about 935 pg/day, about 940 Mg/day, about 945 pg/day, about 950 pg/day, about 955 pg/day, about 960 pg/day, about 965 Mg/day, about 970 pg/day, about 975 pg/day, about 980 pg/day, about 985 pg/day, about 990 pg/day, about 995 pg/day, about 1000 pg/day, about 5 mg/day, about 10 mg/day, about 15 mg/day, about 20 mg/day, about 25mg/day, about 50mg/day, about 75 mg/day, about 100 mg/day, about 125 mg/day, about 150 mg/day, about 175 mg/day, about 200 mg/day, about 225 mg/day, about 250 mg/day, about 275 mg/day, about 300 mg/day, about 325 mg/day, about 350 mg/day, about 375 mg/day, about 400 mg/day, about 425 mg/day, about 450 mg/day, about 475 mg/day, about 500 mg/day, about 525 mg/day, about 550 mg/day, about 575 mg/day, about 600 mg/day, about 625 mg/day, about 650 mg/day, about 675 mg/day, about 700 mg/day, about 725 mg/day, about 750 mg/day, about 775 mg/day, about 800 mg/day, about 825 mg/day, about 850 mg/day, about 875 mg/day, about 900 mg/day, about 925 mg/day, about 950 mg/day, about 975 mg/day, about 1000 mg/day, about 1025 mg/day, about 1050 mg/day, about 1075 mg/day, about 1 100 mg/day, about 1025 mg/day, about 1050 mg/day, about 1075 mg/day, about 1200 mg/day, about 1225 mg/day, about 1250 mg/day, about 1275 mg/day, about 1300 mg/day, about 1325 mg/day, about 1350 mg/day, about 1375 mg/day, about 1400 mg/day, about 1425 mg/day, about 1450 mg/day, about 1475 mg/day, about 1500 mg/day, about 1525 mg/day, about 1550 mg/day, about 1575 mg/day, about 1600 mg/day, about 1625 mg/day, about 1650 mg/day, about 1675 mg/day, about 1700 mg/day, about 1725 mg/day, about 1750 mg/day, about 1775 mg/day, about 1800 mg/day, about 1825 mg/day, about 1850 mg/day, about 1875 mg/day, about 1900 mg/day, about 1925 mg/day, about 1950 mg/day, about 1975 mg/day, about 2000 mg/day, about 2025 mg/day, about 2050 mg/day, about 2075 mg/day, about 2100 mg/day, about 2125 mg/day, about 2150 mg/day, about 2175 mg/day, about 2200 mg/day, about 2225 mg/day, about 2250 mg/day, about 2275 mg/day, about 2300 mg/day, about 2325 mg/day, about 2350 mg/day, about 2375 mg/day, about 2400 mg/day, about 2425 mg/day, about 2450 mg/day, about 2475 mg/day, about 2500 mg/day about 2525 mg/day, about 2550 mg/day, about 2575 mg/day, about 2600 mg/day, about 2625 mg/day, about 2650 mg/day, about 2675 mg/day, about 2700 mg/day, about 2725 mg/day, about 2750 mg/day, about 2775 mg/day, about 2800 mg/day, about 2825 mg/day, about 2850 mg/day, about 2875 mg/day, about 2900 mg/day, about 2925 mg/day, about 2950 mg/day, about 2975 mg/day, about 3000 mg/day, about 3025 mg/day, about 3050 mg/day, about 3075 mg/day, about 3100 mg/day, about 3125 mg/day, about 3150 mg/day, about 3175 mg/day, about 3200 mg/day, about 3225 mg/day, about 3250 mg/day, about 3275 mg/day, about 3300 mg/day, about 3325 mg/day, about 3350 mg/day, about 3375 mg/day, about 3400 mg/day, about 3425 mg/day, about 3450 mg/day, about 3475 mg/day, about 3500 mg/day, about 3525 mg/day, about 3550 mg/day, about 3575 mg/day, about 3600 mg/day, about 3625 mg/day, about 3650 mg/day, about 3675 mg/day, about 3700 mg/day, about 3725 mg/day, about 3750 mg/day, about 3775 mg/day, about 3800 mg/day, about 3825 mg/day, about 3850 mg/day, about 3875 mg/day, about 3900 mg/day, about 3925 mg/day, about 3950 mg/day, about 3975 mg/day, or about 4000 mg/day.
[0076] In some embodiments, the pharmaceutical composition is in dry powder form suitable for administration by dry-powder inhaler. In some embodiments, the pharmaceutical composition is in powder form suitable for administration by metered-dose inhaler. In some embodiments, the pharmaceutical composition further comprises a propellant. In some embodiments, the propellant is 1 ,1 ,1 ,2-tetrafluoroethane.
[0077] In some embodiments, the pharmaceutical composition is in a form suitable for administration by nebulizer. In some embodiments, the pharmaceutical composition is a solution comprising a solvent system. In some embodiments, the solvent system comprises an alcohol. In some embodiments, the solvent system does not include an alcohol. In some embodiments, the solvent system comprises a polyol. In some embodiments, the solvent system does not include a polyol. In some embodiments, the pharmaceutical composition is a suspension.
[0078] In some embodiments, methods of the present disclosure further comprise determining a first forced expiratory volume ("FEV") value of the subject before administering the pharmaceutical composition; and determining a second FEV value of the subject after administering the pharmaceutical composition. In some embodiments, the second FEV value is greater than or substantially greater than the first FEV value. In some embodiments, the first and second FEV values are the volume of air the subject forcibly exhales in 0.5 seconds, 1 .0 second (i.e., "FEVi"), 2.0 seconds or 3.0 seconds.
[0079] In some embodiments, methods of the present disclosure further comprise determining a first FEVi/FVC (forced vital capacity) value of the subject before administering the pharmaceutical composition, and determining a second FEVi/FVC value of the subject after administering the pharmaceutical composition. In some embodiments, the second FEV^FVC value is greater than or substantially greater than the first FEVi/FVC value. In some embodiments, the first FEVi/FVC value is no greater than about 70%. In some embodiments, the second FEVi/FVC value is greater than about 70%. In some embodiments, the first FEVi/FVC value is determined after administration of a bronchodilator medication.
[0080] In some embodiments, the subject is male and the first FEVi/FVC value is no greater than about 88% of a predicted FEVi/FVC value for men having similar age and body composition of said subject. In some embodiments, the subject is female and the first FEVi/FVC value is no greater than about 89% of a predicted FEVi/FVC value for women having similar age and body composition of said subject.
[0081] In some embodiments, the disease or disorder is selected from the group consisting of COPD or asthma. In some embodiments, the disease or disorder is COPD. In some embodiments, the disease or disorder is asthma.
[0082] In some embodiments, methods according to the present disclosure further comprise administering (including co-administering) a second active agent. In some embodiments, the second active agent is selected from the group consisting of: short- acting bronchodilators (i.e. short-acting beta agonists), long-acting bronchodilators (i.e. long-acting beta agonists), phosphodiesterase-4 ("PDE4") inhibitors, corticosteroids, leukotriene receptor antagonists, expectorants and methylxanthines. In some embodiments, the second active agent is co-formulated with the pharmaceutical composition comprising 15-HEPE. In some embodiments, the second active agent is formulated separately and co-administered with the pharmaceutical composition comprising 15-HEPE. As used herein, the term "co-administer" includes administering the second active agent simultaneously, concomitantly, within 1 hour, within 2 hours, within 3 hours, 4 hours, within 5 hours, within 6 hours, within 7 hours, within 8 hours, within 9 hours, within 10 hours, within 1 1 hours, within 12 hours, within 13 hours, within 14 hours, within 15 hours, within 16 hours, within 17 hours, within 18 hours, within 19 hours, within 20 hours, within 21 hours, within 22 hours, within 23 hours, or within 24 hours of the pharmaceutical composition comprising 15-HEPE.
[0083] In one embodiment, the method comprises administering a pharmaceutical composition as disclosed herein once per day, twice per day, three times per day, or more than three times per day.
[0084] In one embodiment, upon treatment in accordance with the present disclosure, for example over a period of about 1 to about 200 weeks, about 1 to about 100 weeks, about 1 to about 80 weeks, about 1 to about 50 weeks, about 1 to about 40 weeks, about 1 to about 20 weeks, about 1 to about 15 weeks, about 1 to about 12 weeks, about 1 to about 10 weeks, about 1 to about 5 weeks, about 1 to about 2 weeks or about 1 week, the treated subject exhibits an improvement in FEV value, an improvement in FCV value, or a combination thereof.
[0085] As used herein, "treating" or "treatment" of a disease, disorder, or condition includes at least partially: (1 ) preventing the disease, disorder, or condition, i.e. causing the clinical symptoms of the disease, disorder, or condition not to develop in a mammal that is exposed to or predisposed to the disease, disorder, or condition but does not yet experience or display symptoms of the disease, disorder, or condition; (2) inhibiting the disease, disorder, or condition, i.e., arresting or reducing the development of the disease, disorder, or condition or its clinical symptoms; or (3) relieving the disease, disorder, or condition, i.e., causing regression of the disease, disorder, or condition or its clinical symptoms. The term "prevention" in relation to a given disease or disorder means: preventing the onset of disease development if none had occurred, preventing the disease or disorder from occurring in a subject that may be predisposed to the disorder or disease but has not yet been diagnosed as having the disorder or disease, and/or preventing further disease/disorder development if already present.
[0086] An "effective amount," as used herein, refers to the amount of an active composition that is required to confer a therapeutic effect on the subject. A "therapeutically effective amount," as used herein, refers to a sufficient amount of an agent or a compound being administered which will relieve to some extent one or more of the symptoms of the disease, disorder, or condition being treated. In some embodiments, the result is a reduction and/or alleviation of the signs, symptoms, or causes of a disease, or any other desired alteration of a biological system. For example, in some embodiments, an "effective amount" for therapeutic uses is the amount of the composition including a compound as disclosed herein required to provide a clinically significant decrease in disease symptoms without undue adverse side effects. In some embodiments, an appropriate "effective amount" in any individual case is determined using techniques, such as a dose escalation study. The term "therapeutically effective amount" includes, for example, a prophylactically effective amount. In other embodiments, an "effective amount" of a compound disclosed herein, is an amount effective to achieve a desired pharmacologic effect or therapeutic improvement without undue adverse side effects. In other embodiments, it is understood that "an effective amount" or "a therapeutically effective amount" varies from subject to subject, due to variation in metabolism, age, weight, general condition of the subject, the condition being treated, the severity of the condition being treated, and the judgment of the prescribing physician. The term "pharmaceutically acceptable" in the present context means that the substance in question does not produce unacceptable toxicity to the subject or interaction with other components of the composition.
[0087] In another embodiment, the present disclosure provides a method of treating, reducing the symptoms of, slowing progression of or promoting regression of a lung disease or disorder such as asthma or COPD.
[0088] In one embodiment, the present disclosure provides a method of reducing or preventing side effects associated with administration of a second active agent. Administration of certain second active agents disclosed herein have been associated with various intolerance symptoms, such as but not limited to: irritation of the oropharynx, mouth, mucus tissues, etc.; headache; nausea; upset stomach; severe allergic reactions (rash; hives; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue); blood in the urine; bloody vomit; diarrhea; dizziness; excitability; fast breathing; fast/irregular heartbeat; flushing; increased thirst or urination; irritability; muscle twitching; pounding in the chest; restlessness; seizures; stomach pain; trouble sleeping; and vomiting. In one embodiment, a method of reducing side effects associated with administration of a second active agent as disclosed herein comprises discontinuing administration of a first pharmaceutical composition comprising the second active agent and administering to a subject a second pharmaceutical composition comprising 15-HEPE as disclosed herein. In one embodiment, the second pharmaceutical composition includes an amount of a second active agent that is less than the amount of the same second active agent in the first pharmaceutical composition. In one embodiment, the second pharmaceutical composition includes an amount of the second active agent that is about equal to or equal to the amount of that second active agent in the first pharmaceutical composition. In one embodiment, the second pharmaceutical composition includes an amount of the second active agent that is more than the amount of that second active agent in the first pharmaceutical composition. In one embodiment, the second pharmaceutical composition does not include the second active agent, essentially none of the second active agent, or substantially none of the second active agent.
[0089] Without further description, it is believed that one of ordinary skill in the art may, using the preceding description and the following illustrative examples, make and utilize the agents of the present disclosure and practice the claimed methods. The following working examples are provided to facilitate the practice of the present disclosure, and are not to be construed as limiting in any way the remainder of the disclosure.
EXAMPLES
Example 1 : In vivo investigation of histamine-induced bronchoconstriction following chronic exposure to 15-HEPE in guinea pigs
[0090] The guinea pig is a reliable animal model in respiratory research due to their respiratory sensitivity and their expression of similar respiratory reactions to those observed in humans. Guinea pigs possess a well-developed bronchial smooth muscle compartment, integral to the purpose of this study.
[0091] This study design was based on current International Conference on Harmonization (ICH) Harmonized Tripartite Guidelines [ICH S7A] and generally accepted procedures for the testing of pharmaceutical compounds.
[0092] Adult male Hartley guinea pigs weighing approximately 450-500 g were acclimated least 5 days before the day of the beginning of the oral gavages. Animals were assigned to one of four groups (low dose, high dose, vehicle and positive control) and were double-housed per group during acclimation period.
A. Preparation of Test Articles solutions
[0093] The test article was formulated using olive oil as the vehicle. A low and a high dose of 15-HEPE (50 mg/kg and 500 mg/kg) was formulated.
B. Preparation of positive control solution
[0094] A 1 mg/ml stock solution of bambuterol was prepared in an aqueous solution, and was then mixed with olive oil in the gavage syringe for the vehicle effect. The stock solution was stored at -20°C, but was used at room temperature and was considered stable for the duration of the experiment.
C. Preparation of the bronchoconstrictor
[0095] A 5 g/ml stock solution of histamine dihydrochloride (Sigma Aldrich) was prepared in a saline solution (0.9% NaCI). The stock solution was stored at 4°C. The expiration date was set at 14 days after preparation.
D. Study Design
[0096] The concentrations of positive control, (bambuterol 0.27mg/kg/day) and the hypertensor (histamine 0.184, 0.919 and 1 .84 pg/kg) were selected based on literature references.
[0097] Each group received the designated compound by oral gavage using a 1 ml syringe. The dosing schedule was as follows:
• Vehicle (olive oil)
• Bambuterol 0.27mg/kg/day
• 15-HEPE 50mg/kg/day
• 15-HEPE 500mg/kg/day
[0098] The stock solutions were administered once per day for seven consecutive days. On the seventh dosage day the animals underwent surgery two hours after the oral feeding. All animal care and vivarium maintenance were recorded, with documents kept at the test facility.
[0099] Guinea pigs were anesthetized with an intraperitoneal injection of urethane (1 .5 g/kg). A tracheotomy was performed and the animals were mechanically ventilated throughout the experiment. The ventilatory pressure was recorded and analyzed for signs of bronchospasm. A pulse oxymeter was attached to each animal's hind paw to obtain heart beat and oxygen saturation on the anaesthetized guinea pigs to continuously monitor the general condition of the animals during the surgical procedure. Following baseline measurements, three doses of histamine (0.184, 0.919 and 1 .84 pg/kg) were nebulized (constant volume tidal, 60 respirations per minute, 7.5 ml/sec), with an interval of 20 minutes between each dose, or until a steady state was reached. Respiratory resistance, heart rate, and oxygen saturation were monitored continuously for a period of about 1 hour post challenge. At the end of the experiment, the animals were euthanized by exsanguination.
E. Results and Analysis
[00100] A networked personal computer running Microsoft Windows was used for data acquisition. The acquisition software was Axoscope 10.2 by Axon Instruments. Axoscope 10.2 has been fully validated in the connected context in which it was used for this study.
[00101] Clampfit 10.2.0.14 analysis software (Axon Instruments), installed on networked personal computers running Microsoft Windows was used. Clampfit 10.2.0.14 has been fully validated in the connected context in which it was used. The graphics software for illustrations is Microsoft Office Excel 2007 installed on networked personal computers running Microsoft Windows. The ventilatory pressure (respiratory resistance) was recorded continuously and was used to calculate the mean respiratory resistance. One-way ANOVAs comparing pre- and post-exposure parameters across experimental groups. Statistical significance confirmed at p < 0.05.
Table 1 : Changes in ventilator pressure (mm Hg) from baseline following nebulized histamine doses after seven consecutive days of gavage with vehicle.
Figure imgf000040_0001
Table 2: Changes in ventilator pressure (mm Hg) from baseline following nebulized histamine doses after seven consecutive days of gavage with bambuterol (0.27 mg/kg/day).
Figure imgf000041_0001
Table 3: Changes in ventilator pressure (mm Hg) from baseline following nebulized histamine doses after seven consecutive days of gavage with 15-HEPE (50 mg/kg/day).
Figure imgf000041_0002
Table 4: Changes in ventilator pressure (mm Hg) from baseline following nebulized histamine doses after seven consecutive days of gavage with 15-HEPE (500 mg/kg/day).
Figure imgf000042_0001
[00102] From the foregoing, it will be appreciated that specific embodiments of the invention have been described herein for purposes of illustration, but that various modifications may be made without deviating from the scope of the invention. Accordingly, the invention is not limited except as by the appended claims.

Claims

CLAIMS I/We claim:
1 . A method for treating a lung disease or disorder comprising administering a
pharmaceutical composition comprising 15-HEPE to a subject in need thereof.
2. The method of claim 1 , wherein the pharmaceutical composition comprises about 50 pg to about 4,000 mg of 15-HEPE.
3. The method of claim 1 or 2, wherein the subject is administered an amount of the composition sufficient to provide about 1 to about 2,000 mg of 15-HEPE to the subject per day.
4. A method for treating a disease or disorder comprising administering a
pharmaceutical composition comprising 15-HEPE to a lung of a subject in need thereof.
5. The method of claim 4, wherein the pharmaceutical composition comprises about 50 pg to about 1 ,000 pg/mL of 15-HEPE.
6. The method of claim 4 or 5, wherein the subject is administered an amount of the composition sufficient to provide about 5 g to about 1 ,000 g of 15-HEPE to the subject per day.
7. The method of any of claims 1 to 6, wherein the disease or disorder is selected from the group consisting of: asthma and COPD.
8. The method of any of claims 1 to 7, wherein the pharmaceutical composition further comprises a second active agent.
9. The method of claim 8, wherein the second active agent is selected from the group consisting of: short-acting bronchodilators, long-acting bronchodilators, phosphodiesterase-4 inhibitors, corticosteroids, leukotriene receptor antagonists, expectorants and methylxanthines.
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